NZ524205A - Key mounting for biological measurement instrument - Google Patents
Key mounting for biological measurement instrumentInfo
- Publication number
- NZ524205A NZ524205A NZ524205A NZ52420598A NZ524205A NZ 524205 A NZ524205 A NZ 524205A NZ 524205 A NZ524205 A NZ 524205A NZ 52420598 A NZ52420598 A NZ 52420598A NZ 524205 A NZ524205 A NZ 524205A
- Authority
- NZ
- New Zealand
- Prior art keywords
- instrument
- user
- key
- keys
- displayed
- Prior art date
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Classifications
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/42—Methods or arrangements for servicing or maintenance of secondary cells or secondary half-cells
- H01M10/425—Structural combination with electronic components, e.g. electronic circuits integrated to the outside of the casing
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/483—Physical analysis of biological material
- G01N33/487—Physical analysis of biological material of liquid biological material
- G01N33/48785—Electrical and electronic details of measuring devices for physical analysis of liquid biological material not specific to a particular test method, e.g. user interface or power supply
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/20—Mountings; Secondary casings or frames; Racks, modules or packs; Suspension devices; Shock absorbers; Transport or carrying devices; Holders
- H01M50/204—Racks, modules or packs for multiple batteries or multiple cells
- H01M50/207—Racks, modules or packs for multiple batteries or multiple cells characterised by their shape
- H01M50/213—Racks, modules or packs for multiple batteries or multiple cells characterised by their shape adapted for cells having curved cross-section, e.g. round or elliptic
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/20—Mountings; Secondary casings or frames; Racks, modules or packs; Suspension devices; Shock absorbers; Transport or carrying devices; Holders
- H01M50/247—Mountings; Secondary casings or frames; Racks, modules or packs; Suspension devices; Shock absorbers; Transport or carrying devices; Holders specially adapted for portable devices, e.g. mobile phones, computers, hand tools or pacemakers
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/20—Mountings; Secondary casings or frames; Racks, modules or packs; Suspension devices; Shock absorbers; Transport or carrying devices; Holders
- H01M50/262—Mountings; Secondary casings or frames; Racks, modules or packs; Suspension devices; Shock absorbers; Transport or carrying devices; Holders with fastening means, e.g. locks
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/20—Mountings; Secondary casings or frames; Racks, modules or packs; Suspension devices; Shock absorbers; Transport or carrying devices; Holders
- H01M50/269—Mechanical means for varying the arrangement of batteries or cells for different uses, e.g. for changing the number of batteries or for switching between series and parallel wiring
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/20—Mountings; Secondary casings or frames; Racks, modules or packs; Suspension devices; Shock absorbers; Transport or carrying devices; Holders
- H01M50/284—Mountings; Secondary casings or frames; Racks, modules or packs; Suspension devices; Shock absorbers; Transport or carrying devices; Holders with incorporated circuit boards, e.g. printed circuit boards [PCB]
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01R—ELECTRICALLY-CONDUCTIVE CONNECTIONS; STRUCTURAL ASSOCIATIONS OF A PLURALITY OF MUTUALLY-INSULATED ELECTRICAL CONNECTING ELEMENTS; COUPLING DEVICES; CURRENT COLLECTORS
- H01R13/00—Details of coupling devices of the kinds covered by groups H01R12/70 or H01R24/00 - H01R33/00
- H01R13/02—Contact members
- H01R13/22—Contacts for co-operating by abutting
- H01R13/24—Contacts for co-operating by abutting resilient; resiliently-mounted
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/50—Current conducting connections for cells or batteries
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Physics & Mathematics (AREA)
- Biomedical Technology (AREA)
- Biophysics (AREA)
- Medicinal Chemistry (AREA)
- Immunology (AREA)
- Computer Hardware Design (AREA)
- Manufacturing & Machinery (AREA)
- Hematology (AREA)
- Molecular Biology (AREA)
- Urology & Nephrology (AREA)
- Food Science & Technology (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Human Computer Interaction (AREA)
- Pathology (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Battery Mounting, Suspending (AREA)
- Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
- Automatic Analysis And Handling Materials Therefor (AREA)
- Electric Clocks (AREA)
- Sampling And Sample Adjustment (AREA)
- Infusion, Injection, And Reservoir Apparatuses (AREA)
- Time Recorders, Dirve Recorders, Access Control (AREA)
- Measurement Of Unknown Time Intervals (AREA)
- Injection Moulding Of Plastics Or The Like (AREA)
- Details Of Connecting Devices For Male And Female Coupling (AREA)
Abstract
The operating keys 54a, b, c of a biological sample measurement instrument extend from a common support 56 mounted in the instrument. Each of the keys has a reduced cross-sectional hinge portion 58 adjacent the common support so that each key can be activated independently of the other.
Description
<div class="application article clearfix" id="description">
<p class="printTableText" lang="en">52 A 2 0 5 <br><br>
Patents Form 5 <br><br>
N.Z. No. <br><br>
NEW ZEALAND Patents Act 1953 COMPLETE SPECIFICATION <br><br>
INSTRUMENT <br><br>
We, ROCHE DIAGNOSTICS CORPORATION, an American Corporation of 9115 Hague Road, Indianapolis, IN 46250, United States of America, do hereby declare the invention, for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement:- <br><br>
-1 - (Followed by 1A) <br><br>
WO 99/28736 1A PCT/US98/25863 <br><br>
INSTRUMENT <br><br>
intellectual property OFFICE OF N.Z. <br><br>
2 7 JAN m received <br><br>
Background of the Invention <br><br>
This is a related application to U.S.S.N. 60/067,512, titled 5 INSTRUMENT, filed December 4, 1997, U.S.S.N. 60/067,499, filed December 4, 1997, titled INSTRUMENT SETUP UTILITY PROGRAM, U.S.S.N. <br><br>
, titled INSTRUMENT, and U.S.S.N. , titled <br><br>
INSTRUMENT SETUP UTILITY PROGRAM, filed on the same date as this application. These related applications are assigned to the same assignee as this 10 application. The disclosures of those applications are incorporated herein by reference. <br><br>
This invention relates to improvements in instalments of the general type described in U. S. Patents: 4,963,814; 4,999,582; 4,999,632; 5,288,636; <br><br>
5,366,609; and, 5,508,171. It is disclosed in the context of such instruments. <br><br>
However, it is believed to be useful in other applications as well. <br><br>
15 Hand held instruments for the determination of physical and biological parameters such as, for example, the concentrations of medically significant components, such as glucose, of biological fluids, such as blood, are in widespread use. Such instruments permit people to monitor such characteristics and treat themselves or take other appropriate action to halt or reverse undesirable trends in the concentrations 20 of such components. In diabetics, for example, such corrective action might be something as simple as intake of a particular type of food, for example, fruit juice, or an injection of insulin In persons who are monitoring a clotting characteristic of their blood, such corrective action might be, for example, taking of a blood thinner or clotting factor. <br><br>
25 <br><br>
Disclosure of the Invention <br><br>
The invention provides an instrument for determining the concentration of a medically significant component of a biological sample, the instrument including first and second keys for use in operating the instrument, the keys extending from a common 3 0 support mounted in the instrument, each of the keys having a reduced cross sectional hinge portion adjacent to the common support whereby substantially independent activation of the first and second keys is provided. <br><br>
oc cu Is" <br><br>
\2Z <br><br>
I u-<° <br><br>
3 tu HO <br><br>
According to another aspect of the invention, an instrument for determining the concentration of a medically significant component of a biological sample includes first and second keys for use in operating the apparatus. The keys extend from a common support mounted in the instrument. Each of the keys has a reduced cross sectional portion adjacent to the common support to promote substantially independent activation of the first and second keys. <br><br>
Illustratively according to this aspect of the invention, the instrument comprises a third key disposed between the first and second keys for use in operating the instrument. The third key also has a reduced cross sectional portion adjacent to a second support mounted in the instrument. <br><br>
Further illustratively according to this aspect of the invention, the common support has a relief portion for receiving the second support such that the three keys generally define a surface when the instrument is assembled. <br><br>
Additionally illustratively according to this aspect of the invention, the instrument includes a housing having first and second portions. The instrument includes a circuit mounted to one of the housing portions and having a set of three terminals. <br><br>
The apparatus further includes means for securing the keys when the first and second ' <br><br>
housing portions are assembled together such that the keys, when activated, operate respective ones of the terminals. <br><br>
Illustratively according to this aspect of the invention, the instrument includes a compressible member disposed between the keys and the terminals of the circuit. <br><br>
Further illustratively according to this aspect of the invention, the compressible member comprises a resilient pad dimensioned to isolate the terminals physically to reduce the possibility of contaminants interfering with the operation of the instrument. <br><br>
Additionally illustratively according to this aspect of the invention, the means for securing the keys comprises pins extending from the other housing portion for reception in a corresponding plurality of openings disposed in the key supports to capture the supports between the other housing portion and the circuit. <br><br>
Other aspects and related inventions are described and claimed in our New <br><br>
Zealand Patent Specification No. 504879, from which the present specification was divided and in other divisional applications. A full description of the interrelated inventions has been retained herewith. <br><br>
3 <br><br>
Brief Description of the Drawings <br><br>
The invention may best be understood with reference to the following detailed description and accompanying drawings which illustrate the invention. In the drawings: <br><br>
5 Fig. 1 illustrates an exploded perspective view of an instrument incorporating the invention; <br><br>
Fig. 2 illustrates an enlarged perspective view of a detail of the instrument illustrated in Fig. 1; <br><br>
Fig. 3 illustrates a further enlarged sectional view, taken generally along 10 section lines 3-3 of Fig. 2, of the detail illustrated in Fig. 2; <br><br>
Fig. 4 illustrates a further enlarged sectional view, taken generally along section lines 4-4 of Fig. 2, of the detail illustrated in Fig. 2; <br><br>
Fig. 5 illustrates an enlarged perspective view of a detail of the instrument illustrated in Fig. 1; <br><br>
15 Fig. 6 illustrates a further enlarged sectional view, taken generally along section lines 6-6 of Fig. 5, of the detail illustrated in Fig. 5; <br><br>
Fig. 7 illustrates a further enlarged sectional view, taken generally along section lines 7-7 of Fig. 5, of the detail illustrated in Fig. 5; <br><br>
Fig. 8 illustrates an enlarged perspective view of a detail of the 20 instrument illustrated in Fig. 1; <br><br>
Fig. 9 illustrates ah enlarged perspective view of a detail of the instrument illustrated in Fig. 1; <br><br>
Fig. 10 illustrates enlarged perspective views of details of the instrument illustrated in Fig. 1; <br><br>
25 Fig. 11 illustrates an enlarged perspective view of a detail of the instrument illustrated in Fig. 1; <br><br>
Figs. 12-13 illustrate enlarged perspective views of a detail of the instrument illustrated in Fig. 1; <br><br>
Fig. 14 illustrates a block diagram of an electric circuit useful in an 30 instrument constructed according to the invention; <br><br>
Figs. 15a-h illustrate partly block and partly schematic diagrams of the electric circuit illustrated in block diagram form in Fig. 14; <br><br>
4 <br><br>
Fig. 16 illustrates a dynamic model of firmware useful in operating the instrument illustrated in Fig. 1; <br><br>
Fig. 17a illustrates the interrupt handling routines executed by firmware useful in operating the instrument illustrated in Fig. 1; <br><br>
5 Fig. 17b illustrates a functional model of firmware useful in operating the instrument illustrated in Fig. 1; <br><br>
Fig. 18 illustrates a detail of the model illustrated in Fig. 17; and, <br><br>
Figs. 19-70b illustrate the user interface of the instrument illustrated in <br><br>
Fig. 1. <br><br>
10 Turning now particularly to Fig. 1, an instrument 20 for the determination of the glucose concentration of blood cooperates with a so-called biosensor strip 21 (Fig. 13) of the general type described in the above identified patents. The instrument 20 includes a case bottom portion 22 (Figs. 1 - 4) and a case top portion 24 (Figs. 1 and 5-7) for housing the remaining components of the 15 instrument 20. A battery door 26 (Figs. 1 and 8) engages bottom portion 22 and encloses two battery wells 28a and b provided in bottom portion 22. Bottom portion 22 and top portion 24 are held together substantially exclusively by the frictional engagement of pins 30 molded into the underside of top portion 24 in complementary sockets 32 molded into bottom portion 22. Slight drafts, for example, about .06 mm 20 along the approximately .6 mm to .7 mm effective heights of sockets 32 and pins 30, are sufficient to facilitate removal of these molded components from their molds, while still providing sufficient frictional engagement to hold top and bottom portions 22, 24 together with the remaining instrument 20 components assembled in them. <br><br>
A well is provided in bottom portion 22 for a brass contact plate 36 for 25 a piezoelectric speaker or buzzer 37 (Fig. 14) which is mounted on the underside of a printed circuit board 38 in instrument 20. A socket 40 is provided on the underside of PCB 38 to make connections to a liquid crystal display 42, the pins 44 of which are inserted into socket 40 through holes 46 provided therefor in PCB 38. This arrangement aids in the manufacture of the circuit board 38 and reduces manufacturing 30 cost. Display 42 illustratively is a 102-by-65 dot matrix LCD. A flexible silicone button pad 48 (Figs. 1 and 9) has terminals or contacts provided on the underside thereof for contact with complementary terminals or contacts 50a-c on PCB 38. The^ <br><br>
tactile cushion portions 52a-c of button pad 48 cooperate with three keys 54a-c (Figs. 1 and 10) mounted on top portion 24 to provide inputs to instrument 20. <br><br>
The two outer keys 54a and c are molded together, but each is joined to f <br><br>
their common support bar 56 by a living hinge 58a, 58c, respectively. Living hinges 5 58a and c are regions of the molded plastic key 54a, c assembly that are somewhat thinner and of reduced width to make the keys 54a, c themselves somewhat more touch sensitive than would be the case without the living hinge structure, and to aid in isolating key presses of key 54a from those of key 54c. Openings 60 are provided in the support bar 56 to receive pins 62 which protrude from the underside of top portion 10 24 to receive the key 54a, c assembly. The remaining key 54b is mounted from a similar support bar 64 by a similar living hinge 58b to permit bar 64 to engage the two middle pins 62. The assembly including the compressible silicone pad 48, key 54a, c assembly, and key54b is captured between the underside of top portion 24 and PCB 38. Again, pins 62 protrude from the underside of top portion 24 to be received in 15 openings 68 provided in bar 64 of key 54b. A depression 69 in bar 56 accommodates bar 64. Key 54b is constructed separately from the keys 54a,c to minimize the spacing between the adjacent surfaces 70 of key 54b and keys 54a and c. The use of the silicone pad 48 and keys 54a-c, and the minimal spacing between adjacent keys 54a-b and b-c help to reduce the possibility of contaminants interferring with the operation of 20 instrument 20. <br><br>
A brass battery contact 74 (Figs. 1 and 11) is press-fitted into a space provided at the back end of bottom portion 22. Contact 74 provides contacts to the opposite terminals of two, for example, 1.5 V, AAA size, dry cells 75 (Fig. 14) which provide power to instrument 20. To prevent the dry cells 75 from being connected 25 backward in the circuit of instrument 20, a boss 76 is molded into bottom portion 22 around the opening 78 through which contact 74 makes contact with the + terminal of the dry cell in well 28a. The dry cell 75 in well 28a will not make contact to the circuit through opening 78 unless the dry cell is inserted in the correct orientation into well 28a. Spring battery contact clips 80 (Figs. 1,12 and 13) are provided at the opposite 30 front ends of both battery wells 28a and b. Each spring battery contact clip 80 <br><br>
includes a base 81 mounted on the PCB 38. Clip 80 turns downward from PCB 38 through a constant radius of illustratively .75 mm to a first leg 82 which extends <br><br>
6 <br><br>
downward from PCB 38 at an angle of between about five degrees and about ten degrees with respect to a line perpendicular to the base portion 81, illustratively about 8°. Clips 80 then turn through a constant radius of illustratively about 1.12 mm and a batteiy-contacting leg 84 extends upward, defining between itself and a perpendicular 5 to base 81 an angle of between about fifteen degrees and about twenty five degrees with respect to the perpendicular, illustratively about 20°. Clips 80 then turn through a constant radius of illustratively about 1mm and a leg 86 extends downward at an angle of between about forty degrees and about fifty degrees with respect to the perpendicular, illustratively about 45°. Clips 80 then turn at a constant radius of 10 illustratively about .75 mm and continue downward to terminate. The total height of clips 80 is about 8.8 mm. This construction reduces the possibility that the clips 80 themselves will be damaged in the event a user drops the instrument 20. Clips 80 illustratively are constructed from half hardened BeCu 190 alloy with a 60/40 tin/lead plating to resist corrosion and ease solder connections. <br><br>
15 A lens 90 (Fig. 1) covers the opening 92 in top portion 24 over LCD <br><br>
42. Lens 90 is constructed from polycarbonate resin with a self-healing polyurethane coating to reduce the degradation of the lens 90's transparency owing to marring of the lens 90 which would otherwise inevitably result from use. A lens constructed from polycarbonate resin with a conventional hard coating to reduce marring may also be 20 used. <br><br>
Top portion 24 includes a slot 94 in its front through which biosensor strips 21 are inserted to initiate tests to determine, inter alia, glucose concentration of blood samples. The strips 21 include, for example, two conductor metallizations extending longitudinally of the strips 21 through which electrical contact is made 25 between the strips' chemistries and the circuitry of the instrument 20. A sockiet 96 through which this contact is made is mounted directly behind slot 94 on PCB 38. Because the slot 94 and socket 96 are provided on separate components of the instrument, 20, namely, the top portion 24 and PCB 38, respectively, some manufacturing tolerance-induced variation in the relative positions of slot 94 and 30 socket 96 is inevitable. Some side-to-side variation is accounted for by ribs 97 (Fig. 7) which extend inward toward the location of socket 96 in the assembled instrument 20. The lower inside regions 99 of ribs 97 are angled slightly away from each other to <br><br>
7 <br><br>
help guide the components of instrument 20 into their designed locations during assembly. Additional accommodation of tolerance-induced variation is provided by the width of the slot 94, the width of the socket 96 and the widths of the electrical . conductor metallizations on the strips 21. Up-and-down tolerance variations are 5 accounted for in part by a pair of spring arms 98 molded into bottom portion 22. <br><br>
Spring arms 98 include upwardly converging somewhat arcuate resilient portions 100 and uppermost contact pads 102 which contact the underside of socket 96 in the assembled instrument 20 Arms 98 help absorb tolerance variations in the up-and-down position of socket 96 with respect to slot 94, urging socket 96 gently upward in 10 those instances in which it is at the low point of its assembly tolerance so that strips 21 will slide easily through slot 94 into and from socket 96. Arms 98 also stabilize the front portion of PCB 38 against shock caused by incidental jarring of the instrument 20 during use. <br><br>
Turning now to Figs. 14 and 15a-h, the electric circuit of the instrument 15 20 includes a microcontroller (jiC) 110 (Fig. 14 and Fig. 15c) and an application-specific integrated circuit (ASIC) 112 (Fig. 14 and Fig. 15a), as well as other discrete and integrated circuit components. In the description that follows, specific discrete and integrated circuit components, and in many instances, specific sources of these components, will be identified. The circuit will be described with reference to those 20 specifically identified components, sometimes referring to terminals by terminal names and numbers and/or pin numbers. This should not be interpreted to mean that these are the only components available from the identified sources or any sources which will perform the necessary functions in the circuit. Indeed, typically there will be a number of suitable discrete and integrated circuit components available from the identified 25 sources and other sources which will perform the necessary functions. Some of such substitute components will use the same terminal/pin identifiers as those noted in this description. Others, however, will use different designations. <br><br>
Referring now particularly to Fig. 14 and Fig. 15a, socket 96 is illustrated as including four terminals 96-1—96-4 which are coupled through an EMI 30 filter to the SENSOR EXCITing, SENSOR FeedBack, SENSOR INput, and <br><br>
CONTACT 2 INput terminals, respectively, of ASIC 112. These terminals are all constrained to be * - .6 V and < ASIC VDD + .6 V by respective diodes 114. ASIC <br><br>
8 <br><br>
VDD is provided from the system VDD supply through a 39 Q resistor and the source and drain of an FET 116. FET 116 illustratively is a type BSS84 FET. Terminals 96-3 and -4 are also coupled through respective series 10 KQ resistors and 1 §iF capacitors to form the STRIP IN EXCITe and STRIP IN ChecK terminals of the instrument 20. 5 These terminals are used by the instrument 20's operating system to turn the instrument 20 on in response to the insertion into slot 94 of a biosensor strip. Terminal 96-3 is also coupled through a 4.99 KQ resistor to the CALibrate Resistance EXCITe terminal of ASIC 112, and through a 7.5 KQ resistor to the IV AMPlifier FeedBack terminal of ASIC 112. Terminal 96-4 is also coupled through a 49.9 KQ resistor to 10 ground. Instrument 20's ASIC CLocK PoWeR is coupled to the power supply terminal of an inverter 117. The input terminal of inverter 117 is coupled to instrument 20's ASIC CLocK terminal. The output terminal of inverter 117 is coupled through a 100 Q resistor to ASIC 112's XIN terminal. The ASIC clock frequency of 153.6 KHz is a submultiple (1/32) of the system clock frequency (4.9152 MHz) and is 15 derived from the system clock. Inverter 117 illustratively is a type TC7SHU04 <br><br>
inverter. The TEMPerature SIGnal INput terminal of ASIC 112 is held at a 1.235 V voltage reference level by, for example, an LT1004-1.235 voltage reference IC. ASIC 112 illustratively is the same type ASIC as is used in the Accu-Chek® Advantage® instrument available from Boehringer Mannheim Corporation, 9115 Hague Road, 20 Indianapolis, Indiana 46250-0457. <br><br>
Referring now to Fig. 14 and Fig. 15b, the battery + connector 80b, which forms instrument 20's V BATT terminal, is coupled through a 470 nH inductor <br><br>
119 to the collector of a switching regulator transistor 120. The emitter of transistor <br><br>
120 is coupled to battery - connector 80a, the instrument 20 ground. The base of 25 transistor 120 is coupled through a 20 KQ resistor to ground. As a second function, <br><br>
the collector of transistor 120 is coupled to an inverter and multiplier comprising a diode 121, the anode of which is coupled through a .33 ^F capacitor to the collector of transistor 120 and the cathode of which is coupled to ground, and a diode 123, the cathode of which is coupled to the anode of diode 121 and the anode of which is 30 coupled through a .33 \iF capacitor to ground and forms the instrument 20's notVEE terminal. This terminal nominally runs at about -3 .5 VDC. Terminal 80b is also coupled through inductor 119 and the parallel combination of a 5.1 V Zener diode and <br><br>
a Schottky diode to form the VDD terminal of instrument 20. A 10 jiF capacitor is coupled across VDD and ground. Transistor 120 switching of VBATT through inductor 119 permits VDD to run nominally at about 5.1 VDC. The emitter of a transistor 122 is coupled to VDD. Its collector is coupled through a 5.1 V Zener 5 diode to ground. Its base is coupled through a 20 KQ resistor to VDD and through a 2 KQ resistor to the instrument 20's notCLAMP DRIVE terminal. The emitter of a transistor 124 is coupled through a 2 KQ resistor to VDD. Its collector is coupled to the base of transistor 120. The base of transistor 124 is coupled through a 20 KQ resistor to instrument 20's notSWitching REGulator DRIVE terminal to drive 10 transistor 120 with a pulsewidth modulated waveform to regulate the power supply voltages. The PWM pulse repetition frequency is a submultiple (1/128) of the system clock frequency (4.9152 MHz) and is derived from the system clock to minimize the possibility of beat frequencies which could deleteriously affect the performance of instrument 20. The voltage is monitored by monitoring VDD and VBATT voltages 15 through the ^C 110 A/D port. The pulse width is modulated by nC 110 in a closed loop control strategy to maintain the desired voltage. Transistor 120 illustratively is a type 2N3904 transistor. Transistors 122 and 124 illustratively are type MMBT3906 transistors. <br><br>
Terminal 80b is also coupled through a 2 MQ resistor to the INput 20 terminal of a voltage monitor IC 126. The OUTput terminal of IC 126 forms the instrument 20's nC 110 notRESET terminal. The VCC and GrouND terminals of IC 126 are coupled across the instrument 20's Real Time Clock VDD and ground terminals. A parallel RC circuit including a .1 nF capacitor and a 2.74 MQ resistor is coupled across the IN and GND terminals of IC 126. IC 126 illustratively is a type 25 MAX836 voltage monitor IC. <br><br>
Referring now to Fig. 14 and Fig. 15d, the instrument 20's real time clock includes a real time clock IC 128 whose VDD and GrouND terminals are coupled across RTC VDD and ground. RTC VDD is coupled to IC 128's Frequency Output Enable terminal. The Frequency SELect terminal of IC 128 is coupled to 30 ground. The series string of a 1 KQ resistor 130, a 100 KQ resistor 132, the drain of an FET 134, the source of FET 134 and a 20 KQ resistor is coupled between RTC VDD and ground. The instrument 20's SuperCAPacitor SAMPle terminal is coupled <br><br>
10 <br><br>
to the source of FET 134. The instrument 20's SuperCAPacitor SWitch terminal is coupled through a 100 KQ resistor to the gate of FET 134. This configuration permits the charge state of a .047 nF capacitor 137 coupled between the junction of resistors 130,132 and ground to be managed. The voltage across capacitor 137 is measured 5 whenever the instrument 20 is awakened to check for a strip insertion to verify that a minimum voltage level is present by turning on the resistor 130, 132 voltage divider network. If this voltage level drops below the required level, the switching regulator of Fig. 15b is maintained on until the next strip insertion check. This strategy is implemented because the reset generator 126 and the real time clock 128 require a 10 minimum supply voltage of 2.5 VDC, while the battery voltage may go as low as 2.2 VDC in a working instrument 20. The DATA, ClocK, WRite, and Chip Enable terminals of IC 128 form instrument 20's RTC DATA, RTC CLK, RTC WR, and RTC CE terminals, respectively. The Frequency OUT terminal of IC 128 is coupled through series inverting amplifiers 140, 142 and a 100 Q resistor to the XT2 terminal 15 ofuCl 10. The output terminal of inverter 140 is coupled through a 100 Q resistor to the XT1 terminal of ftC 110. IC 128 illustratively is an Epson type RTC4543SA 32 KHz real time clock IC. <br><br>
Referring back to Fig. 15 a, instrument 20 includes a port 140 for receiving a key which carries a ROM containing, inter alia, lot-specific parameters for 20 the biosensor strips 21 currently in use in the instrument 20. Port 140 includes terminals 140-1 — 140-8. Terminals 140-1 — 140-4 and 140-8 are coupled through respective 100 0 resistors to the instrument 20's Code ROM CS terminal, CR ClocK terminal, TXD1 terminal, RXD1 terminal and CR VCC terminal, respectively. Terminal 140-7 is coupled through a ferrite bead to V BATT. Terminal 140-5 is 25 coupled to instrument 20 ground. The purposes and functions of such code ROM keys are explained further in U. S. Patent 5,053,199. The code ROM on the key which port 140 is adapted to receive illustratively is a National Semiconductor type NMC93C56 or C66 ROM. <br><br>
Keys 54-a — c are coupled to \iC 110's ports 04 — 06, respectively (Fig 30 14c). Ports 00-03 form instrument 20's ASIC Code ROM Chip Select, ASIC EEPROM Chip Select, ASIC CR DATA OUT and 232 IN terminals, respectively. Interieaved conductor patterns 144 form instrument 20's humidity sensor. One set of <br><br>
11 <br><br>
these interleaved patterns 144 is coupled to ground. The other set is coupled to the fiC 1 10's port 17 and through a 100 KQ resistor to pC 110's analog reference input at the collector of a transistor 146. The emitter of transistor 146 is coupled to V BATT. The base of transistor 146 is coupled through a 20 KQ resistor to V BATT and 5 through a 20 KQ resistor to pC 110's port 127. V BATT operating potential, stepped down by a 100 ICQ resistor to a 1.2 V voltage reference 147, is coupled to ports 10 — 12 of nC 110. Ports 13 and 14 of pC 110 form the SCAP SAMP and STRIP IN CK terminals, respectively of instrument 20. Ports 15 and 16 are coupled through a 100 KQ resistor to instrument 20's VDD SAMPle terminal. Ports 20 — 23 form the 10 instrument 20's RXD1, TXD1, CR CLK and CR CS terminals, respectively. pC 110 illustratively is an NEC pPD78P058 eight-bit microcontroller Transistor 146 illustratively is a type MMBT3906 transistor. <br><br>
The interior of instrument 20 is fairly crowded. As a result, some heating effects result when instrument 20 is operated in certain of its modes over 15 extended times. The chemistries which reside on typical biosensor strips 21 are somewhat temperature dependent. Prior art instrument designs have taken this into consideration by providing temperature sensors and algorithms which adjust their biosensor strip outputs for ambient temperature. However, further temperature correction has been found advantageous in instrument 20. Specifically, it has been 20 found that, as instrument 20 operates in certain modes, heat builds up in the instrument. This results in a difference between ambient temperature, that is, the temperature of strip 21 and the temperature against which the reaction of the chemistry on strip 21 must be compensated to provide an accurate glucose concentration reading, and the temperature measured by the thermometer mounted on PCB 38 inside 25 the instrument 20. pC 110 uses an algorithm which takes into account how long instrument 20 has been operating in each of its several different heat-evolving modes since it was last turned on to calculate how much adjustment to an indicated ambient temperature is appropriate in order to provide a more accurate calculated glucose concentration. Amounts of adjustment for heat buildup in instrument 20 range from 0 30 to about 2.5% or so. The algorithm will be explained in detail later. The temperature sensor itself includes a digital thermometer IC 150 (Fig. 14 and Fig.l5a). An illustrative digital thermometer is the Dallas Semiconductor DS1621C IC. Instrument <br><br>
12 <br><br>
20's TEMPerature ClocK and TEMPerature DATA terminals are coupled through respective 100 Q resistors to the SCL and SDA terminals, respectively, of the digital thermometer 150. The SCL and SDA terminals of digital thermometer 150 are also coupled to the SCL and SDA terminals, respectively, of a serial EEPROM IC 152. 5 Serial EEPROM 152 illustratively is an Atmel type AT24C256 serial EEPROM IC. The WP terminal of serial EEPROM 152 is coupled through a 100 Q resistor to port 24 of jiC 110. Power is supplied to ICs 150, 152 from instrument 20's TEMPerature VCC terminal through a 100 Q resistor. A 10 KQ resistor is coupled between the VDD and SDA terminals ofIC 150. In this configuration, the digital thermometer 150 10 and EEPROM 152 are time-division multiplexed onto the same bus into nC 110. <br><br>
Referring back to Fig. 14 and Fig. 15c, ports 25 and 27 of nC 110 form instrument 20's TEMP DATA and TEMP CLK terminals, respectively. Ports 30 — 36 form instrument 20's notSW REG DRIVE, RTC CE, RTC WR, RTC CLK, RTC DATA, ASIC CLK and piezoelectric BUZzer OUTput terminals, respectively. Ports 15 40 — 47 form instrument 20's Display 0 — Display 7 terminals, respectively. Referring to Fig. 14 and Fig. 15d, terminals DO — D7 are coupled through respective 100 Q resistors to terminals 40-3 — 40-10, respectively, of socket 40. The notDISPlay Chip Select 1, DISPlay AO, notReaD, notWRite and notDISPlay RESET terminals of instrument 20 are coupled through respective 100 Q resistors to terminals 40-1,40-2, 20 40-11,40-12 and 40-13, respectively, of socket 40. Display 42 is powered through an FET 153, the source of which is coupled to VDD and the drain of which is coupled to the power supply terminals 40-14 and -15 of socket 40. The gate of FET 153 is coupled through a 100 KQ resistor to the instrument 20's notDISPlay ON terminal. Display 42 may be backlit to ease reading of it. The notBacKLight ON terminal of 25 instrument 20 is coupled through a 2 KQ resistor to the base of a transistor 154. The emitter of transistor 154 is coupled to V BATT. V BATT is coupled through a 2 KQ resistor to the base of transistor 154.The collector of transistor 154 is coupled to the power supply terminal of an inverter 156. The input terminal of inverter 156 is coupled to instrument 20's ASIC CLK terminal. The collector of transistor 154 is 30 coupled through respective 100 Q resistors to terminals 40-18 and 40-19 of socket 40. The output terminal of inverter 156 is coupled through a 100 Q resistor to terminal 40-19 of socket 40. FET 153 illustratively is a type BSS84 FET, transistor 154 <br><br>
13 <br><br>
illustratively is a type MMBT3906 transistor, and inverter 156 illustratively is a type TC7SHU04 IC inverter. <br><br>
Figs. 15g-h illustrate the LCD display module schematics. The display controller 157, which illustratively is a SMOS SED1560, includes two sets of terminals 5 VI-V5, pins 6 and 46, 5 and 47, 4 and 48, 3 and 49, and 2 and 50, respectively, coupled through respective 1 nF, 16 V capacitors to Vcc. The VDD, M/S, SCL, SI, P/S, CS2 and T2 terminals, pins 7, 8, 10, 11, 12, 14 and 35, respectively, of display controller 157 are coupled to Vcc. The C86, Vss, CLear, and T1 terminals, pins 15, 19 and 37, 32, and 36, respectively of display controller 157 are coupled to ground. The 10 D0-D7 terminals, pins 20-27, respectively, of display controller 157 are coupled to the system D0-D7 lines. The OSC1 and OSC2 terminals, pins 34 and 33, are coupled together through a 1MQ, 1% resistor. The CAP1+ and CAP1- terminals, pins 38 and 39, are coupled together through a 1 fiF, 16 V capacitor. The CAP2+ and CAP2-terminals, pins 40 and 41, are coupled together through a 1 jiF, 16 V capacitor. The 15 VOUT terminal, pin42, is coupled to ground through a 2.2 jiF, 16 V capacitor. The V5 terminal, pin 43, is coupled through series 340KQ, 1% and 47KQ resistors to the VR terminal, pin 44, of display controller 157. The VR terminal is also coupled through a 102KQ, 1% resistor to Vcc. The VDD terminal, pin 45, is coupled to V^. Pins 1-13 of a connector 159 provide access to the notCSl, AO, D0-D7, notReaD, 20 notWRite, and notRESet terminals, pins 13, 16, 20-27,11, 12, and 13, respectively, of display controller 157. VcC is coupled to pins 14 and 15 of connector 159. Ground is coupled to pins 16 and 17 of connector 159. Pins 18-20 of connector 159 are reserved for LED backlight connections for display 42. This permits two LED backlight anode connections, A1 and A2, to a common LED cathode return, K. Pins 1-20 of 25 connector 159 are coupled to terminals 40-1—40-20, respectively. Alternatively, pins 18-20 of connector 159 can be used to drive an electroluminescent (EL) backlight, as illustrated in Fig. 15h. In this alternative embodiment, pin 18 of connector 159 forms the EL Vcc terminal and pin 20 forms the EL VCc ground terminal. Parallel .01 §j.F and 4.7 |jF bypass capacitors are coupled across pins 18 and 20. Pin 19 is coupled to the 30 CAPacitor2 terminal of an EL backlight driver IC 161, such as, for example, a SIPEX SP4422ACN IC. A 150 pF capacitor may optionally be coupled across the CAP2 and CAP1 terminals of driver 161 to cause it to operate at a frequency other than the <br><br>
14 <br><br>
ELOSC frequency appearing at pin 19. The HON and Vdd terminals of driver 161 are coupled to EL Vcc. The COIL terminal of driver 161 is coupled through an inductor, for example, a 9 mH shielded inductor, to EL Vcc. The Vss terminal of driver 161 is coupled to EL Vcc ground. The EL backlight can then be coupled across the ELI and 5 EL2 terminals of driver 161. <br><br>
Referring now to Fig. 14 and Fig.l5e, instrument 20 includes an RS232 I/O port 160 including terminals 160-1 — 160-3. Terminal 160-1 is coupled to ground. Terminal 160-3, instrument 20's RS232 port receive terminal, is coupled through a 20 KQ resistor to the base of a transistor 162. A parallel RC circuit 10 including a .001 jiF capacitor and a 100 KQ resistor is coupled between the base of transistor 162 and ground. The emitter of transistor 162 is coupled to ground. Its collector forms instrument 20's 232 INput terminal. Its collector is coupled through a 20 KQ load resistor to VDD. Instrument 20's 232 OUTput terminal is coupled through a 20 KQ resistor to the base of a transistor 164. The emitter of transistor is 15 coupled to VDD. The collector of transistor 164 is coupled to the bases of a transistor 166 and a transistor 168. The emitters of transistors 166, 168 are joined. The collector of transistor 166 is coupled to VDD and the collector of transistor 168 is coupled to instrument 20's notVEE terminal. The joined emitters of transistors 166, 168 are coupled through a 100 Q resistor to terminal 160-2, instrument 20's RS232 20 port transmit terminal. A 20 KQ pull-up resistor is coupled between VDD and the base of transistor 164. A 10 KQ pull-down resistor is coupled between the base of transistor 168 and notVEE. Transistors 164,168 illustratively are type MMBT3906 transistors. Transistors 162, 166 illustratively are type 2N3904 transistors. <br><br>
Referring back to Fig. 15c, ports 50 — 53 of nC 110 form instrument 25 20's ASIC CR CLK, ASIC CR DATA IN, ASIC CLK PWR and DROP DETECT terminals, respectively. Ports 55 — 57 and 60 form instrument 20's notDISPlay RESET, notDISPlay Chip Selectl, DISPlay AO, and notBacKLight ON terminals, respectively. Instrument 20's notCLAMP DRIVE terminal is formed by ports 61 —63 of nC 110. Ports 64 and 65 of nC 110 form instrument 20's notReaD and notWRite 30 terminals. Ports 70 and 71 of jiC 110 are coupled to instalment 20's 232 IN and 232 OUT terminals, respectively. Ports 120 — 125 form instrument 20's TEMP VCC, <br><br>
jf <br><br>
15 <br><br>
VDD SAMP, CR VCC, notASIC ON, SCAP SW and notDISP ON terminals, respectively. <br><br>
Referring now to Fig. 14 and Fig 15f, port 126 of fiC 110 is coupled through a 100 KQ resistor to the gate of an FET 170. The source of FET 170 is 5 coupled to VDD. The drain of FET 170 is coupled through a 1 KQ resistor to the collector of a transistor 172. The emitter of transistor 172 is coupled to ground. The base of transistor 172 is coupled through a 20 KQ resistor to instrument 20's piezoelectric BUZzer OUTput terminal. The collector of transistor 172 forms one, 174-1, of the buzzer 37 output terminals. The emitter of a transistor 176 is coupled to 10 the drain of FET 170. The collector of transistor 176 is coupled through a 1 KQ <br><br>
resistor to ground. The base of transistor 176 is coupled through a 20 KQ resistor to the collector of transistor 172. The collector of transistor 176 forms the other buzzer 37 output terminal 174-2. Terminals 174-1 and -2 are clamped £ - .6 V and <, VDD + .6 V. FET 170 illustratively is a type BSS84 FET. Transistor 172 illustratively is a 15 type2N3904. Transistor 176 illustratively is a type MMBT3906. <br><br>
Referring back to Fig 15c, port 130 of jiC 110 forms the STRIP IN EXCIT terminal of instrument 20. A 4 .9152 MHz crystal clock is coupled across ports XI — X2 of nC 110. The notRESET port of \iC 110 forms instrument 20's MPU RESET terminal and is coupled through a 10 KQ resistor to VDD. 20 Returning to the instrument 20's internal heating algorithm, the internal heating can be described by a first-order differential equation, <br><br>
x(dv/dt) + v = T(Temp., Pwr.) (1) <br><br>
25 in which x is a heating/cooling time constant which is determined empirically and varies depending upon the internal geometry of the instrument 20 and other factors, v is the correction value, dv/dt is the rate of change of the correction value with respect to time, and T(Temp., Pwr.) is the steady state difference between ambient temperature outside the meter (that is, the temperature of the strips 21 and the 30 chemistries on those strips) and the temperature inside the instrument 20 as reported by digital thermometer 150. Equation 1 can be represented as a difference equation: <br><br>
16 <br><br>
v(t + At) = v(t) - (At/r) * v(t) + (At/r) * T(Temp., Pwr.). (2) <br><br>
For the illustrated instrument 20, x(heating) is 20 minutes, t(cooling) is 15 minutes, At(cooling) is 2 seconds, At(heating) is 1 second, T(Temp., Pwr.) with the instrument 20 in its "sleep" state is 0 (since the temperature differential between the ambient temperature and the digital thermometer 150's indicated temperature approaches 0 with increasing time in the sleep state), and T(Temp., Pwr.) in each of the instrument 20's active, heat-evolving states is stored in a look-up table in EEPROM 152. <br><br>
Equation 2 is scaled as illustrated in equation 3. Equation 3 is implemented in instrument 20's firmware to calculate the correction factor: <br><br>
v(t + At) * 25600 = v(t) * 25600 + <br><br>
{ - [(At/r) * 131072] *[v(t) * 25600]/32768 +[(At/t) * T(Temp., Pwr.) * 102400]}/4 <br><br>
(3) <br><br>
Values for T(Temp., Pwr.) are stored for each of three temperature ranges, namely: Temp. < 20°C; 20°C £ Temp. < 30°C; and Temp. £ 30°C; and for each of four different power consumptions, namely: low power consumption (low clock speed with backlight ofi); low clock speed with backlight on; high clock speed with backlight off; and, high power consumption (high clock speed with backlight on). Useful meter internal temperature correction values can be determined from these values. For the illustrated instrument, useful T(Temp., Pwr.) values are listed in the following table. It should be understood, however, that these values will vary with the internal configuration and operating parameters of the instrument. <br><br>
Ambient Temperature <br><br>
Power Level, P <br><br>
low clock speed with backlight off low clock speed with backlight on high clock speed with backlight off high clock speed with backlight on <br><br>
<20°C <br><br>
0 <br><br>
0.43 <br><br>
0.68 <br><br>
0.93 <br><br>
20°C z Temp. <30°C <br><br>
0 <br><br>
0.60 <br><br>
0.68 <br><br>
0.93 <br><br>
Temp, i 30°C <br><br>
0.28 <br><br>
0.73 <br><br>
0.68 <br><br>
0.93 <br><br>
/ <br><br>
. j <br><br>
■H _/ <br><br>
17 <br><br>
Fig. 16 illustrates the dynamic model of the interaction of the firmware which is programmed into pC 110's internal ROM. The circles indicate the various states of fiC 110. The firmware is primarily interrupt driven. To increase battery life when the ^C 110 is not servicing an interrupt or processing pending events, pC 110 is 5 maintained in an idle state When the pC 110 is in idle state, the clock speed is lowered from 4.9152 MHz to 32 KHz. When the program monitor is in the wakeup state, it is determining what caused the wakeup interrupt. When it is in the monitor state, it is processing serial commands. When it is in the ready state, it is waiting for user input. When it is in the periodic service state, it is performing periodic tasks, such 10 as checking for a strip insertion or updating the instrument 20's temperature history. When it is in ASIC service state, it is processing a request from the ASIC 112, such as a request for data from the EEPROM 152 or the ROM key interface 140, or receiving information from the ASIC 112. When in test state, it is performing a test, either a blood glucose determination, a control glucose determination, or a diagnostic using a 15 check strip. In the reset state, it is performing a power on reset initialization. In the idle state, it is halted awaiting wakeup. In the error state, it is handling some type of system error. In the user interface service state, it is processing a reaction to a key 54 press. In the data management service state, it is retrieving or storing data. <br><br>
The various interrupts and the pC 110's responses to them are 20 illustrated in Fig. 17a. The reset interrupt vectors to the reset state. The ASIC 112 Code ROM Chip Select interrupt handles ASIC code ROM 140 chip selects. The routine receives a code ROM 140 address from the ASIC, vectors to a routine to read the contents of the specified address, and sends the contents to the ASIC 112. This interrupt is only enabled when the ASIC 112 is on. This interrupt occurs when the 25 instrument 20 is in the test state, or when the instrument 20 is in the monitor state and the pass through command has been issued. <br><br>
The ASIC 112 EEPROM 152 Chip Select interrupt handles EEPROM 152 commands from ASIC 112. The routine receives a read command, an enable write command or a write command. The EEPROM read command reads an 30 EEPROM address from the ASIC, retrieves the data from the pC 110 RAM (to which it has previously been transferred by the firmware), formats it, and sends it to the ASIC 112. The EEPROM enable write command reads the full command from the ASIC <br><br>
18 <br><br>
112. The EEPROM write command gets an EEPROM 152 address and data from the ASIC 112 and stores this address and data in the nC 110's RAM It should be noted that the EEPROM 152 contents are loaded into the nC 110's RAM before the ASIC 112 is powered up. The ASIC 112 EEPROM CS interrupt is only enabled when the 5 ASIC is turned on. This interrupt occurs when the instrument 20 is in the test state, or when the meter is in the monitor state and the pass through command has been issued. <br><br>
The process ASIC 112 code ROM 140 data output interrupt handles ASIC serial data that is received. This routine only processes data received from the ASIC 112 if the code ROM and EEPROM chip selects are not selected. This routine 10 vectors to a routine to read the ASIC 112 data and store the received data in the nC 110's serial data buffer. This interrupt determines if the ASIC 112 has sent all expected data for the pending command, and if so, signals an appropriate event. This interrupt is only enabled when the ASIC 112 is turned on. This interrupt occurs when the insturment 20 is in the test state, or when the instrument is in the monitor state and 15 the pass through command has been issued. <br><br>
The process RS-232C data input interrupt wakes up the ^C 110 when external data is input. This function sets the appropriate event to receive data via the HC 110's built-in Universal Asynchronous Receiver-Transmitter from the RS-232C port 160. This interrupt is only enabled when the instrument 20 is in the idle state. 20 The process button interrupt sets the appropriate event to handle a key <br><br>
54a-c press. This interrupt is enabled when the instrument 20 is in the idle state, or when the instrument 20 is turned on and the display 42 prompts the user to make soft key 54 choices. <br><br>
The process UART receive error interrupt handles UART errors. The 25 error indicator is cleared and the UART is reset. The nC 110's serial I/O buffer is cleared. This interrupt is enabled except when the instalment 20 is in the idle state. <br><br>
The process UART receive complete interrupt processes a byte received via the UART. Depending on the state of the ^C 110, the firmware monitor state and the data received, the data may be stored in the nC 110's serial I/O buffer 30 and/or may be echoed back to the sender. This interrupt is enabled except when the instrument 20 is in the idle state. <br><br>
I <br><br>
■J <br><br>
19 <br><br>
The process UART transmit complete interrupt sends data via the UART and manages the serial I/O buffer. This interrupt is enabled except when the instrument 20 is in the idle state. <br><br>
The process periodic wake up timer interrupt causes the instrument 20 5 to wake from the idle state to check for a strip 21 insertion and/or to update the instrument 20's temperature history when appropriate. This interrupt is enabled when the instrument 20 is in the idle state. <br><br>
The process erroneous interrupt should not be used. However, if it is, <br><br>
the user is notified if possible. The instrument 20 then sets an error state and is <br><br>
\ <br><br>
10 inoperable until the batteries 75 are removed from the instrument 20 and reinserted or replaced with new batteries to force a reset. This interrupt is always enabled. <br><br>
The functional model of the firmware is illustrated in Fig. 17b. Power on reset is entered through the reset interrupt. States of the instrument 20 at the beginnings of the various functions are indicated in parentheses. The instrument 20 15 initializes itself by: initializing the stack pointer, resetting the jiC 110 ports to the power up reset state; configuring the ports/resources for proper use; checking the battery level to be sure that it is sufficient for operation; setting the }iC 110 terminals to the power up reset state; initializing the pC 110's RAM; initializing the instrument 20's components to power up steady state; initializing the instrument 20's power 20 management system; loading the contents of EEPROM 152 into |iC 110 RAM; incrementing a power up reset counter; initializing the instrument 20's temperature history; code ROM 140 cyclic redundancy checks, checking the manufacturing data flags to be sure that they are set, and checking the EEPROM 152 data (dynamic text, current language, etc.) to determine that it is correct; sending a power up reset 25 complete acknowledgement; and, producing an audible beep on speaker 37 to indicate to the user that power up has been completed. <br><br>
The set wake up sources function sets the port terminals and components to the power down terminal state and sets the interrupts for possible wake ups. The sleep function sets the clock to low clock speed and places the pC 110 in 30 halt mode. The wake up function is initiated via interrupts to indicate what events require service. Appropriate event flags are set within the interrupt routines. The system OK? function performs system level failsafes: the condensation sensor; <br><br>
20 <br><br>
SuperCAPacitor status; and, EEPROM 152 cyclic redundancy check (calibration, <br><br>
status, setup and insulin pump). This function also increments the power up counter, readies the instrument 20 for further processes by starting the main clock and resetting the stack pointer, and checks the battery level to be sure it is sufficient. <br><br>
5 As previously noted, the process system error interrupt should never have to be used. However, if it is, the user is notified, if possible. Then the instrument 20 sets itself to an error state from which it is inoperable until the batteries are removed and reinserted or replaced with new batteries. <br><br>
The any events pending? function determines if any events are pending 10 and need to be handled. If no events are pending, the nC 110 monitors the PWM voltage and waits for a pending event or timeout. If the (iC 110 is waiting for user input or serial input and the time to system timeout elapses, the nC 110 returns to idle state. <br><br>
The process periodic events function checks whether there are any 15 events that should be processed, such as: charging the SuperCAPacitor; performing a temperature sample; updating the temperature history; adjusting the internal self-heating variable; and, checking for a test strip 21 insertion. <br><br>
The inactivity timeout elapsed? function operates while waiting for a button press or for serial data. This function determines if a timeout has occurred. If 20 so, the nC 110 is put back into the idle state. <br><br>
The process pending events function is illustrated in Fig. 18. The following actions take place when the pC 110 processes a pending event. The process button press event function is invoked when a button is pressed. This function has a delay that permits the user to press more than one button simultaneously. Then the 25 function samples the buttons' states, saves the buttons'states and provides feedback to the user about which buttons are pressed. Based upon the current screen state, the appropriate screen handler routine is used for further processing. If a button is not pressed, the button press event is cleared. <br><br>
The process poll button event function provides a fast key 54 press 30 feature. A key 54a-c is pressed and held down. If the fast mode is active, the status of each key 54a-c is polled. If a pressed key 54a-c is in fast mode, feedback to the user is <br><br>
21 <br><br>
provided. Then the appropriate screen handler routine is employed. If a key 54a-c is pressed but not held down, the associated function, such as + or - is invoked. <br><br>
The process serial wake up event occurs when the RS-232C wake up interrupt has been triggered. The current instrument 20 state is checked. If the 5 instrument 20 is in idle state, the instrument 20's state is changed to monitor state and an acknowledgement is sent to the interrupt source. If the instrument 20 is not in idle state, the wake up is ignored and the pending event is cleared. <br><br>
The process serial data event occurs when the UART receives a complete interrupt and determines whether the data in the serial I/O buffer should be 10 processed further. If the data is a complete command, the UART detects the end of a data block, or the ASIC pass through mode is enabled, the routine to process data in the serial I/O buffer is invoked and the pending event is cleared. <br><br>
The process strip insert event occurs when the periodic timer wake up determines that a strip 21 has been inserted. The power management system and LCD 15 are initialized and permitted to stabilize. The routine to run a glucose test is invoked. The pending event is cleared. <br><br>
The process periodic service event occurs when the periodic timer wake up determines that it is time to perform a temperature sample, update the termperature history, adjust the internal self-heating variable, regulate power management (check 20 the status of the power management and make adjustments when necessary), or check the timeout counters. <br><br>
The user interface of instrument 20 will now be explained with reference to Figs. 19-73. Referring particularly to Fig. 19, when screen 200 is displayed and the user presses key 54a, the function for option 1, for example, "RUN 25 GLUCOSE TEST," of instrument 20 is executed. When screen 200 is displayed and the user presses key 54b, instrument 20 is turned off. When screen 200 is displayed and the user presses key 54c, screen 202 offering option 2, for example, "REVIEW MEMORY," is displayed. The user advances in the same manner, scrolling up additional options 3, for example, "EDIT/ENTER DATA," 4, for example, "SET 30 DATE AND TIME," 5, for example, "SET OPTIONS," 6, for example, "CHECK BATTERY," and so on, until the last option is displayed. <br><br>
22 <br><br>
Turning now to Fig. 20, when screen 204 listing the last option is displayed and the user presses key 54a, the function for the last option, in the illustrated example, option 6, of instrument 20 is executed. When screen 204 is displayed and the user presses key 54b, instrument 20 is turned off. When screen 204 5 is displayed and the user presses key 54c, the option menu rolls over to option 1 and screen 200 is displayed. <br><br>
Turning now to Fig. 21, and assuming that the instrument 20 is in the off state, insertion of batteries 75 into the instrument 20 will place the instrument 20 in the power up reset state. See Fig. 22. If the time has elapsed prior to a periodic wake 10 up, the instrument 20 will be placed in wake up state. See Fig. 23. If the user presses any button 54a-c, the instrument 20 will be placed in the wake up state. See Fig. 24. If instrument 20 detects serial data from, for example, port 160, the instrument 20 is placed in the wake up state. See Fig. 25. <br><br>
Immediately upon power up, instrument 20 performs its power up 15 checks, illustrated in Fig. 26. These include the battery level check, illustrated in Fig. 27a. If the battery level is not sufficient to run instrument 20, the screen illustrated in Fig. 27b is displayed. From this screen, the user may turn the instrument 20 off until the batteries can be serviced by pressing key 54b. Alternatively, the instrument 20 will power itself off after passage of the timeout interval. If the battery 75 level is below a 20 warning threshold, a battery warning icon is set in the display 42, advising the user that the batteries 75 need to be replaced. Ater performing the battery level check, the instrument 20 performs its memory checks illustrated in Fig. 28a. If instrument 20 fails its memory checks, the screen illustrated in Fig 28b is displayed. From this scren, the user may turn the instrument 20 off until the instrument 20 can be serviced. 25 Alternatively, the instrument 20 will power itself off after passage of the timeout interval. <br><br>
After performing the memory check, if a language has previously been selected, that selection is followed. If no language has previously been selected, the instrument executes its language selection routine for the language for its displays. See 30 Figs. 29a-b which illustrate the routine and the display prompt to the user. After the language for displays has been established, the instrument determines whether it needs <br><br>
! <br><br>
23 <br><br>
to have its real time clock reset. If so, appropriate prompts are provided. If not, control is returned to the background program. <br><br>
Before performing a measurement, the instrument 20 must check the code ROM key in port 140 (see Figs. 31a-f), take a temperature reading, and perform 5 certain self-diagnostic tests. See Fig. 30a. The instrument 20 proceeds to the temperature determination. If the ambient termperature is outside the lock out limits of instrument 20, the error message of Fig. 30b is displayed. From this error message, the user can either turn the instrument 20 off or return to the menu. The instrument 20 next proceeds to determine if the temperature is within the warning limits. If so, a 10 temperature warning icon is displayed. The instrument 20 next proceeds to perform its self diagnostic tests. If it passes these tests, it prompts the user to insert a test strip 21 (see Figs. 32a-c). If not, it displays the error screen illustrated in Fig. 30c. From this error message, the user can either turn the instrument 20 off or return to the menu. <br><br>
Turning to Figs. 31 a-f, port 140 is checked to determine if a code ROM 15 key is inserted into it. If not, the missing code key screen illustrated in Fig. 3 lb is displayed. From this error message, the user can either turn the instrument 20 off or return to the menu. If a code key is in the port 140, the type of key is determined. If the type of key is incorrect, an incorrect code key message is displayed. See Fig. 31c. From this error message, the user can either turn the instrument 20 off or return to the 20 menu. If the correct type of code key is in port 140, the integrity of the code key's ROM contents is checked. If the code key ROM contents are corrupt, a code key damaged message is displayed. See Fig. 31 d. From this error message, the user can either turn the instrument 20 off or return to the menu. If the code key ROM contents are viable, the code number of the code key is displayed for the user to compare to the 25 code printed on the vial of strips from which the user will take a strip 21 for a glucose test. See Fig. 31 e. The instrument 20 next determines from the information contained in the code key ROM whether the strips 21 associated with that code key are expired. If so, a strips expired message is displayed. Fig. 3 If. From this error message, the user can turn the instrument 20 off, return to the menu, or conduct a test using the 30 expired strip 21. If the user elects to conduct a test using the expired strip 21, an expired strip warning icon is set on the display 42, and the instrument 20 returns to the <br><br>
24 <br><br>
background routine. If the strips have not expired, the instrument 20 returns to the background routine. <br><br>
Turning now to the strip prompt routine illustrated in Fig 32a, the instrument first determines if a strip 21 is already in the strip port 96. If not, the user is 5 prompted by the display 42 to insert one. See Fig. 32b. The user may also advance from the display of Fig. 32b by turning instrument 20 off or by returning to the menu. If a strip 21 is already in port 96, or the user inserts one in response to the display of Fig. 32b, the instrument 20 next determines the type of strip inserted, based upon certain electrical characteristics of the strip. The firmware contemplates three 10 possibilities: a good diagnostic, or check, strip; a good test strip; or, a bad strip. If the strip is determined by instrument 20 to be bad, a bad strip message is displayed. See Fig. 32c. From this error message, the user can turn the instrument 20 off, return to the menu, or remove the strip, at which time the instrument 20 again prompts for the insertion of a strip. See Fig. 32b. <br><br>
15 If the instrument 20 determines that the inserted strip 21 is a good one, <br><br>
the instrument 20 prompts the user to apply blood to the target area of the strip 21. Figs. 33a-b. The user can escape by turning the instrument 20 off or by returning to the main menu, or the user can apply blood to the strip 21. If the user applies blood to a strip 21, the instrument 20 displays the testing screen. See Fig. 33c. This screen 20 includes a gauge which indicates approximately the percentage completion of the test and a message, or tip, from among a library of programmed tips. These messages crawl across a message line of the display in the illustrated instrument 20. The instrument 20 performs the glucose concentration determination. If an error is detected in the performance of this determination, an error message is displayed. See 25 Fig. 33d. From the detection of such an error, the user can turn the instrument 20 off, return to the main menu or remove the strip. If the strip is removed, the strip prompt, Figs 32a-b, is displayed. If no error is detected, the instrument proceeds to display the measurement on the display 42. See Fig. 33e. The user can respond to the display of the measurement by permitting the instrument 20 to time itself out and power down, 30 by returning to the main menu, by removing the strip, by selecting to enter events associated with the just completed measurement, or by selecting the diary for entry of the just completed measurement. <br><br>
25 <br><br>
The performance of the measurement will be described with reference to Figs 34a-e. Referring particularly to Fig. 34a, the instrument 20's measurement engine is started, temperature data is provided to the measurement engine, the glucose measurement is calculated and stored, and control is returned to the background 5 routine. During the performance of the measurement, if the strip 21 is removed from port 96, or if the code ROM key is removed from port 140, an error screen is displayed. See Figs. 34b-d. The type of error is indicated in the display of Fig. 34d. This is the meaning of the X's in Fig. 34d. The user can respond to the display of Fig. 34d by turning the instrument 20 off or by returning to the main menu. Figs. 34b-c. If 10 the strip 21 has been removed during performance of the measurement, the display 42 prompts the user to insert a strip 21. If the measurement results in an excessive glucose concentration indication, a different screen is displayed. That screen is illustrated in Fig. 34e, the glucose overflow error screen. <br><br>
Turning now to the options available in the main menu, and with 15 reference to Figs. 35a-c, selection of the main menu by the user causes a main menu screen to be displayed. The user may scroll through the options available from the main menu by pressing key 54c. The screen continues to roll over until all available options from which the user may select have been displayed. See Figs. 35b-c. The user may select from among these available options as indicated in the flowchart 20 illustrated in Fig. 35a. The options include: running a glucose test (Figs.32a-c, 33a-e and 34a-e); reviewing the contents of the instrument 20's memory (Figs.36a-d); editing the memory menu and making entries to it (Figs. 46a-d); setting the date and time (Figs. 60a-c); setting the options (menu) (Figs. 61a-c); and, checking the battery (Figs. 69a-b). <br><br>
25 Running a glucose test has previously been described. Reviewing memory can best be illustrated by referring to 36a-d. If the user elects to review memory, a screen is displayed from which the user can select from among the various memory files. See Figs. 36b-c. The user scrolls down through the various memory files until the one the user wishes to review is highlighted. One of the file options is a 30 return to the main menu. The remaining file options include the options to review: diary; prior glucose test results; test results trends; a graph of selected glucose test <br><br>
26 <br><br>
results; glucose ranges; the number of hypoglycemic events recorded in the memory; glucose averages; and, insulin pump profiles for insulin pump users. <br><br>
If the user selects the review diary option, the screen illustrated in Fig. 37b is displayed. The user is permitted to review multiple events in each diary entry, 5 and the most recently entered events are displayed first. The user may scroll up to earlier entered events. Fig. 37c. Events include, for example: type and time duration of various forms of exercise (Fig. 37d); carbohydrate intake (Fig. 37e); amounts of each of a number of different types of insulin taken (Fig. 37f); and, amounts of certain other biologically significant components (in the illustrated examples, ketones —Fig. 10 37g, and glycosylated hemoglobin —Fig. 37h) detected in the samples applied to strips 21 (of course, the strips 21 must be capable of providing reliable indications to the instrument 20 of any such components). The display 42 denotes any out of limits results with exclamation marks (!). <br><br>
If the user selects the review glucose option, the screen illustrated in 15 Fig. 3 8b is displayed. The user may scroll up to data from earlier readings and down to more recent readings. No readings other than glucose concentration test results are displayed under this option. Any applicable warnings, such as temperature out of range at the time of measurement, glucose concentration out of range, and so on, are displayed with the glucose readings. <br><br>
20 If the user selects the review trend option, the screen illustrated in Fig. <br><br>
39b is displayed. This screen has rows representing days on which readings are stored in memory, with each day being divided into a number of columns representing a number of time segments of the 24 hour day. In the illustrated instrument 20, the user can divide the day into eight segments according to the user's own treatment regimen, 25 habits, and so on, but the entire 24 hours of each day must be accounted for. In the illustrated instrument 20, the eight columns are somewhat arbitrarily labelled: BReaKfast; MidMOrning; LUNch; MidAFteraoon; DINner; EVEning; BEDtime; and, NiGhTtime. Illustratively, the corresponding time intervals might be, for example: 6:00 am— 8:59 am; 9:00 am — 11:59 am; 12:00 noon —1:59 pm: 2:00 pm — 4:59 pm; 30 5:00 pm — 7:59 pm; 8:00 pm - 9:59 pm; 10:00 pm - 2:59 am; and, 3:00 am - 5:59 am, respectively. As previously noted, the time interval width, starting time and ending time of each column are user selectable, as will be explained. In the illustrated <br><br>
% <br><br>
27 <br><br>
instrument 20, out of range readings are displayed in reverse video, with light numbers on a dark background. <br><br>
If the user selects the graph option, a graph of results will be displayed. See Fig. 40b. In the illustrated instrument 20, the x axis represents forty-eight hours 5 with divisions every six hours. The scale of the y axis is 50 — 350 mg/dL with a division each 100 mg/dL in this range. The user's normal range can be entered, as will be discussed, and, if entered will be indicated by dotted lines. Values within the user's range are illustrated by + symbols. Values outside the instrument 20's reading range range low are illustrated by V symbols. Values outside the instrument 20's reading 10 range high are illustrated by A symbols. The user may scroll forward and back using keys 54c and 54a, respectively, and values forward and back in time from the displayed 48 hours will appear on the graph. <br><br>
If the user selects the glucose ranges option, the user is asked to select a date range for records to be viewed. In the illustrated instrument 20, the user may 15 select the last thirty days, the last fourteen days, the last seven days or the last forty-eight hours. The screen illustrated in Fig. 41b will be displayed with the date range displayed at the top of the display. The display will display the percentage of hypoglycemic test results, and the number of total test results in the date range. If the user presses key 54c, additional records including the percentage of low readings, the 20 percentage of readings in the normal range, the percentage of high readings, and, <br><br>
again, the total number of test results in the date range, will be displayed. See Fig. 41c. The date range is selected as illustrated in Figs. 42a-b. The user selects the date screen, illustrated in Fig. 42b, and scrolls down using key 54c until the desired date range is highlighted. The user then selects that date range using key 54a. The 25 instrument then returns to the routine illustrated in Fig. 41a. <br><br>
If the user selects the number of hypoglycemic events option, the user is asked to select the date range over which the number of hypoglycemic events will be reported. See Figs. 42a-b. Once the user has selected a date range, the screen illustrated in Fig. 43b is displayed. In the illustrated instrument, the number of 30 hypoglycemic events is reported by time of day. See the above discussion of Figs. 39a-b. The user can scroll down and up among the number of hypoglycemic events reported by time of day by pressing keys 54c and 54a, respectively. <br><br>
28: <br><br>
If the user selects the review averages option, the user is again asked to select the date range over which the averages will be calculated. See Figs 42a-b. <br><br>
Once the user has selected a date range, the screen illustrated in Fig. 44b is displayed. In the illustrated instrument, the averages are reported by time of day. See the above 5 discussion of Figs. 39a-b. The user can scroll up and down among the averages reported by time of day by pressing keys 54a and 54c, respectively. <br><br>
If the user selects the review insulin pump profile option, the screen illustrated in Fig. 45b is displayed. Other insulin pump information, such as temporary basal rates, bolus and square wave bolus, is illustrated with other information when the 10 review diary option is selected. <br><br>
Returning briefly to Fig. 35a, the user may edit and enter in the main data menu as illustrated in Figs. 46a-d. If the user selects this option, the screen illustrated in Fig. 46b is displayed. The user may scroll down among the options on the main data menu by pressing key 54c, See Figs. 46c-d. The menu rolls over when 15 the last screen is reached. The user selects a highlighted option by pressing key 54a. The options in the illustrated instrument 20 include; diary; insulin types; insulin pump operating parameters; carbohydrate intake; events; exercise; ketones; glycosylated hemoglobin; and, return to the main menu. <br><br>
To edit and enter diary, the flowchart illustrated in Fig. 47a is 20 instructive. First, the date and time are selected. Once the user has selected the date and time in which the user is interested, the diary settings for that date and time are displayed beginning with the display illustrated in Fig. 47b. The user may advance through the various screens for that date and time by pressing key 54c. The user may recall previous screens by pressing key 54b. See Figs. 47c-f. The user may change a 25 diary entry by pressing key 54a, and then selecting the entry to be changed by pressing key 54b to advance the highlighting of the entries. See Fig. 47g. Once the entry to be changed is highlighted, the user can increase the entry value by pressing key 54c or decrease the entry value by pressing key 54a until the appropriate value is displayed. See Figs. 47h-k. The save key appears on the last screen, Fig. 47f. The user cannot 30 save changed data until all screens, Figs. 47b-f, have been displayed. <br><br>
The user is prompted to select the date and time by the display of the screen illustrated in Fig. 48b. The user may scroll up to earlier entries using key 54c. <br><br>
29 <br><br>
In the illustrated instrument, the screen illustrated in Fig. 48b is only displayed when the user enters the routine illustrated in Fig. 46a. <br><br>
To edit or enter insulin settings, the user first selects the date and time (see Figs 48a-b), and then views the current insulin settings on the display illustrated 5 in Fig. 49b. Pressing key 54c saves the displayed settings. No other action saves them. Pressing key 54a permits the user to edit or enter new settings. The user selects the setting to be edited or entered by depressing key 54b until that setting is highlighted. The user presses key 54a to reduce that setting and presses key 54c to increase that setting. <br><br>
10 If the user elects the insulin pump option in Fig. 46a, the insulin pump menu screen illustrated in Fig. 50b is displayed on display 42. The user may select from the insulin pump menu options by scrolling down through the options using key 54c until the desired option is highlighted, and then pressing key 54a to select that option. The user may then: edit or enter data into the bolus settings as illustrated in 15 Figs. 51 a-c; edit or enter data into the temporary basal settings as illustrated in Figs. 52a-c; edit or enter data into the square wave bolus settings as illustrated in Figs. 53a-c; or, edit or enter basal profiles as illustrated in Figs. 54a-i. <br><br>
If the user elects to edit or enter the bolus settings, the user is first prompted to select the date and time. See Figs. 48a-b. The bolus setting for the 20 selected date and time is then displayed. See Fig. 51b. Pressing key 54c saves the displayed setting. No other action saves it. If the user wishes to change the displayed setting, the user presses key 54a. The setting is highlighted. See Fig. 51c. The user increases the setting by pressing key 54c, and reduces it by pressing key 54a. When the correct setting is reached, the user presses key 54b and then key 54c and the new 25 setting is entered. <br><br>
If the user elects to edit or enter temporary basal settings, the user is first prompted to select the date and time. See Figs 48a-b. The temporary basal setting for the selected date and time is then displayed. See Fig. 52b. Pressing key 54c saves the displayed setting. No other action does. If the user wishes to change the 30 displayed setting, the user presses key 54a. A field of the setting is highlighted. See Fig. 52c. If the highlighted field is the field the user wishes to change, the user increases the setting by pressing key 54c, and reduces it by pressing key 54a. When <br><br>
30 <br><br>
the correct setting is reached, the user presses key 54b and then key 54c and the new setting is entered. If the highlighted field is not the field the user wishes to change, the user may advance to the field he or she wishes to change by pressing key 54b until the setting the user wishes to change is highlighted. <br><br>
5 If the user elects to edit or enter square wave bolus settings, the user is first prompted to select the date and time. See Figs. 48a-b. The square wave bolus setting for the selected date and time is then displayed. See Fig. 53b. Pressing key 54c saves the displayed setting. No other action does. If the user wishes to change the displayed setting, the user presses key 54a. A field of the setting is highlighted. See 10 Fig. 53c. If the highlighted field is the field the user wishes to change, the user increases the setting by pressing key 54c, and reduces it by pressing key 54a. When the correct setting is reached, the user presses key 54b until the screen illustrated in Fig. 53b is displayed, and then key 54c, and the new setting is entered. If the highlighted field is not the field the user wishes to change, the user may advance to the 15 field he or she wishes to change by pressing key 54b until the field the user wishes to change is highlighted. <br><br>
If the user elects to edit or enter basal profiles, the user is first prompted to select the date and time. See Figs. 48a-b. The basal profiles for the selected date are then displayed, beginning with the screen illustrated in Fig. 54b. The 20 user may scroll forward and back through the profiles for the selected date by pressing keys 54c and 54b, respectively. The user may save the current settings for the selected date by pressing key 54c when the last screen is displayed. See Fig. 54e. No other action saves the current settings. To change the current settings, the user presses key 54a. A field of the settings is highlighted. See Fig. 54f. If the highlighted field is the 25 one the user wishes to change, the user presses key 54c to increase the setting, and key 54a to decrease it. When the correct setting is reached, the user presses key 54b until the screen illustrated in Fig. 54b is displayed, and then key 54c through the screens illustrated in Figs. 54c-e, and the new setting is entered. If the highlighted field is not the field the user wishes to change, the user may advance to the field he or she wishes 30 to change by pressing key 54b until the field the user wishes to change is highlighted. <br><br>
Returning to Fig. 46a, if the user elects the edit/enter carbohydrates option, the user is first prompted to select the date and time. See Figs. 48a-b. The <br><br>
31 <br><br>
carbohydrates setting for the selected date and time is then displayed. See Fig. 55b. Pressing key 54c saves the displayed setting. No other action does. If the user wishes to change the displayed setting, the user presses key 54a. The screen illustrated in Fig. 55c is displayed The user increases the setting by pressing key 54c and decreases it by 5 pressing key 54a. When the correct setting is displayed, the user presses first key 54b to display the screen illustrated in Fig. 55b, and then key 54c to save the changed entry. <br><br>
Returning to Fig. 46a, if the user elects the edit/enter events option, the user is first prompted to select the date and time. See Figs. 48a-b. The screen 10 illustrated in Fig. 56b is displayed. Pressing key 54c advances through the event screens. See Fig. 56c. Pressing key 54c when screen 56c is displayed saves the displayed settings. No other action does. If the user wishes to change a displayed setting, the user presses key 54a, The screen illustrated in Fig. 56d is displayed. If the highlighted field is the one the user wishes to change, the user presses keys 54a and c 15 to scroll through the various available event texts Until the correct one is displayed, <br><br>
then presses key 54b until the display illustrated in Fig. 56b is displayed, then key 54c until the changed entry is saved. <br><br>
Returning to Fig. 46a, if the user elects the edit/enter exercise option, the user is first prompted to select the date and time. See Figs. 48a-b. The screen 20 illustrated in Fig. 57b is displayed. Pressing key 54c when screen 60b is displayed saves the displayed settings. No other action does. If the user wishes to change a displayed setting, the user presses key 54a, and the screen illustrated in Fig. 57c is displayed. If the highlighted field is the one the user wishes to diange, the user presses keys 54a and c to scroll through the various available exercise texts until the correct 25 one is displayed, then presses key 54b, returning to the display illustrated in Fig. 57b. The user then presses key 54c to save the changed entry. <br><br>
Returning to Fig. 46a, if the user elects the edit/enter ketones option, the user is first prompted to select the date and time. See Figs. 48a-b. The screen illustrated in Fig. 58b is then displayed. Pressing key 54c when the screen illustrated in 30 Fig. 58b is displayed saves the displayed settings. No other action does. If the user wishes to change the displayed settings, the user presses key 54a, and the screen illustrated in Fig. 58c is displayed. The user presses keys 54a and c to scroll through <br><br>
32 . <br><br>
the various ketones texts until the correct one is displayed, and then presses key 54b, returning to the display illustrated in Fig. 58b. The user then presses key 54c to save the changed entry. <br><br>
Returning to Fig. 46a, if the user elects the edit/enter glycosylated 5 hemoglobin, the user is first prompted to select the date and time. See Figs. 48a-b. The screen illustrated in Fig. 59b is then displayed. Pressing key 54c when the screen illustrated in Fig. 59b is displayed saves the displayed settings. No other action does. If the user wishes to change the displayed settings, the user presses key 54a, and the screen illustrated in Fig. 59c is displayed. The user presses keys 54a and c until the 10 correct entry is displayed, and then presses key 54b, returning to the display illustrated in Fig. 59b. The user then presses key 54c to save the changed entry. <br><br>
The user may need to set the correct date and time, for example, when the batteries 75 have been out of the instrument 20 for more than an hour or so, discharging the supercapacitor. Other date and time parameters, such as, for example, 15 whether the user prefers a twelve hour clock or a twenty-four hour clock, or whether the user prefers the date displayed as day, month and year or as month, day and year, are also user selectable. If the user selects the set date and time option from Fig. 35b, the date and time screen illustrated in Fig. 60b is displayed. Pressing key 54c when the screen illustrated in Fig. 60b is displayed saves the displayed settings. No other action 20 does. If the user wishes to change the displayed settings, the user presses key 54a, and the screen illustrated in Fig. 60c is displayed. If the highlighted field is the one the user wishes to change, the user presses keys 54a and c until the correct field is displayed. The user then presses key 54b to return to the display illustrated in Fig. 60b, and then presses key 54c to save the corrected date and time. If the highlighted field is not the 25 one the user wishes to change, the user presses key 54b to advance through the fields until the one the user wishes to change is highlighted. <br><br>
If the user selects the set options menu from Fig. 3 5c, the screen illustrated in Fig. 61b is displayed. The user may select from among several options in the illustrated instrument 20, including: meter options; insulin; insulin pump; glucose 30 ranges; setting the time blocks; setting the diary; and, country (language) options. The user can scroll downward through the various options using key 54c. Pressing key 54a when a particular option is highlighted results in entiy into a routine to set that option. <br><br>
it- <br><br>
{•5 \ <br><br>
i <br><br>
33 <br><br>
For example, and with reference to Figs. 62a-c, the user can elect to have the buzzer 37 power switch 170 enabled or disabled, the backlight power switch 154 enabled or disabled, and the scrolling messages or tips enabled or disabled. If the user elects to view the meter options, the screen illustrated in Fig. 62b is displayed. Pressing key 54c 5 when the screen illustrated in Fig. 62b is displayed saves the current meter setup options. No other action does. If the user wishes to change the meter setup options, he or she presses key 54a. This results in the display of the screen illustrated in Fig. 62c. The user may change the setup of the highlighted option by pressing either key 54a or key 54c. Pressing key 54b through all of the remaining options returns the user 10 to the screen illustrated in Fig. 62b. Pressing key 54c saves the changed setup options. If the highlighted option in Fig. 62c is not the one the user wishes to change, the user may press key 54b to advance through the available options until the one the user wishes to change is highlighted. <br><br>
If the user elects the set insulin option from Fig. 61a, the screen 15 illustrated in Fig. 63b is displayed. Pressing key 54c displays for the user the screen illustrated in Fig. 63c. If the user wishes to save these settings, he or she may do so by pressing key 54c. No other action will save these settings. If the user wishes to change any of these settings he or she may press key 54a. The screen illustrated in Fig. 63d will be displayed. If the highlighted setting is the one the user wishes to change, 20 the user may press keys 54a and c until the setting is changed to the appropriate new setting. The user can then press key 54b until the screen illustrated in Fig. 63b is displayed, and then press key 54c until the new settings are saved. If the highlighted setting is not the one the user wishes to change, the user may press key 54b until the highlighted setting is the one the user wishes to change. <br><br>
25 If the user elects the insulin pump option from Fig. 61 a, the screen illustrated in Fig. 64b is displayed. If the user wishes to save this setting, he or she may do so by pressing key 54c. No other action will save this setting. If the user wishes to change this setting, he or she may press key 54a. The setting will be changed. Pressing key 54c will save the changed setting. <br><br>
30 If the user elects the set glucose ranges option from Fig. 61 a, the screen illustrated in Fig. 65b will be displayed. If the user wishes to save these settings, he or she may do so by pressing key 54c. No other action will save these settings. If the <br><br>
34 <br><br>
user wishes to change these settings, he or she may press key 54a. The screen illustrated in Fig. 65c will be displayed. If the highlighted setting is the one the user wishes to change, the user may change the setting by pressing one of keys 54a and 54c until the correct setting appears in the highlighted area. The user then presses key 54b until the display returns to the screen illustrated in Fig. 65b. The user then presses key 54c to save the correct setting. If the highlighted setting is not the one the user wishes to change, the user presses key 54b until the highlighted setting is the one to be changed, and proceeds as described above. <br><br>
If the user elects the set time blocks option from Fig. 61a, the screen illustrated in Fig. 66b will be displayed. The user may refer back and forth between the screen illustrated in Fig. 66b and the screen illustrated in Fig. 66c by pressing key 54c when the screen of Fig. 66b is displayed and key 54b when the screen of Fig. 66c is displayed. The user may save the settings of Figs. 66b-c by pressing key 54c when the screen of Fig. 66c is displayed. No other action will save these settings. If the user wishes to diange the times in any blocks, the user may press key 54a. The screen illustrated in Fig. 66d will be displayed. If the user wishes to change the highlighted entry, the user may do so by pressing keys 54a and 54c until the desired entiy appears in the highlighted area. The user may then advance through the remaining entries, one at a time, making any other desired changes to the remaining entries as they are highlighted, in the same manner as the changes were made to the first highlighted entry. In the illustrated instrument 20, only the beginning times of the various time blocks are user selectable. The ending times are calculated by the instrument 20 to be one minute before the starting times of the next subsequent time blocks and are entered automatically by the instrument 20. After the last entiy is highlighted, and changed if 25 desired, pressing key 54b will return the display to screen 66b. To save the changes, the user need only press key 54c to display screen 66c, and then press key 54c again to save the changes. <br><br>
If the user elects the set diary defaults option from Fig. 61 a, the screen illustrated in Fig. 67b will be displayed. Pressing key 54c will scroll the display down 30 until the time block whose diary default settings are to be changed is highlighted. If the user wishes to change any of the diary default settings for a highlighted time block, the user presses key 54a. The screen illustrated in Fig. 67c is displayed. The user may <br><br>
s4, w <br><br>
35 <br><br>
move back and forth among the various screens illustrated in Figs. 67c-g by pressing keys 54c to advance to the next subsequent screen (Figs. 67c-f only) and 54b to go back to the immediately preceding screen (Figs 67d-g only). The user may save the current diary default settings by pressing key 54c when the screen illustrated in Fig. <br><br>
5 67g is displayed. No other action will save the current settings. If the user wishes to change the current settings, the user need only press key 54a and the screen illustrated in Fig. 67h will be displayed. The user may change the highlighted entry by pressing keys 54a and c until the highlighted entry is correct. If the highlighted entry is not to be changed, the user may advance through the entries by pressing key 54b until the 10 entry to be changed is highlighted. The user may then change that entiy as described above. Pressing key 54b after the last entry illustrated in Fig. 671 is highlighted returns the user to the screen illustrated in Fig. 67c. The corrected diary default settings are then saved by advancing to the screen illustrated in Fig. 67g and pressing key 54c. <br><br>
If the user elects the set country option from Fig. 61a, the screen 15 illustrated in Fig. 68b is displayed. If the user does not wish to change the settings, the user may press key 54c and save the settings. If the settings are saved, the routine checks to be sure that a different language has been selected for the user interface. If not, control is returned to the set options menu. If a different language has been selected, the instrument 20 is powered down. If the user wishes to change any setting, 20 the user presses key 54a. The screen illustrated in Fig. 68c is displayed. The user can advance through the available options for the highlighted setting by pressing keys 54a and 54c until the desired option appears. The user may then press key 54b to highlight the next setting, and then press keys 54a and 54c if any change is desired in the next highlighted option. The user may continue to do this until pressing key 54b returns the 25 user to the screen illustrated in Fig. 68b. The user then presses key 54c to save the revised settings. <br><br>
If the user selects the check battery option from Figs. 35a-c, the screen illustrated in Fig. 69b is displayed. The shading of the battery in the screen corresponds to the batteries 75s' voltage. The user may return from this display to the 30 main menu, turn the instrument 20 off, or permit to time itself off. <br><br>
Referring to Figs. 70a-b, the illustrated instrument also keeps track of certain additional events and parameters. Pressing of keys 54a-c simultaneously causes <br><br>
36 <br><br>
the screen illustrated in Fig. 70b to be displayed. This screen displays the instrument 20's serial number (Sisssssss), the version of the firmware with which the instrument 20 is operating (V :v.w), the number of times the instrument 20 has been powered up (Ciailll), the number of glucose concentration determinations the instrument 20 has run (C2:22222) and the number of times the instrument 20 has been reset (C3:33333). <br><br>
37 <br><br></p>
</div>
Claims (8)
1. An instrument for determining the concentration of a medically significant component of a biological sample, the instrument including first and second keys for use in operating the instrument, the keys extending from a common support mounted in the instrument, each of the keys having a reduced cross sectional hinge portion adjacent to the common support whereby substantially independent activation of the first and second keys is provided.<br><br>
2. The instrument of claim 1 further comprising a third key disposed between the first and second keys for use in operating the instrument, the third key also having a reduced cross sectional hinge portion adjacent to a second support mounted in the instrument.<br><br>
3. The instrument of claim 2 wherein the common support has a relief portion for receiving the second support such that the three keys generally define a surface when the instrument is assembled.<br><br>
4. The instrument of claim 3 including a housing having first and second portions, the instrument including a circuit mounted to one of the housing portions and having a set of three terminals, the instrument further including means for securing the keys when the first and second housing portions are assembled together such that the keys, when activated, operate respective ones of the terminals.<br><br>
5. The instrument of claim 4 including a compressible member disposed between the keys and the terminals of the circuit.<br><br>
6. The instrument of claim 5 wherein the compressible member comprises a resilient pad dimensioned to isolate the terminals physically to reduce the possibility of contaminants interfering with the operation of the instrument.<br><br>
7. The instrument of claim 4 wherein the means for securing the keys comprise pins extending from the other housing portion for reception in a corresponding plurality of openings disposed in the key supports to capture the supports between the other housing portion and the circuit.<br><br>
8. An instrument according to claim 1 substantially as herein described or exemplified.<br><br> ROCHE DIAGNOSTICS CORPORATION By Their Attorneys HENRY HUGHES Per:<br><br> intellectual property<br><br> OFFICE OF N.Z.<br><br> 27 JAN 2004 RECEIVED<br><br> </p> </div>
Applications Claiming Priority (2)
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US6751297P | 1997-12-04 | 1997-12-04 | |
NZ504879A NZ504879A (en) | 1997-12-04 | 1998-12-04 | Instrument for engaging a power cell |
Publications (1)
Publication Number | Publication Date |
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NZ524205A true NZ524205A (en) | 2004-05-28 |
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Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
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NZ504879A NZ504879A (en) | 1997-12-04 | 1998-12-04 | Instrument for engaging a power cell |
NZ524206A NZ524206A (en) | 1997-12-04 | 1998-12-04 | Instrument for determining the concentration of a medically significant component of a sample |
NZ524205A NZ524205A (en) | 1997-12-04 | 1998-12-04 | Key mounting for biological measurement instrument |
NZ524204A NZ524204A (en) | 1997-12-04 | 1998-12-04 | Instrument for the determination of physical and biological parameters such as temperature and concentration of glucose |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
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NZ504879A NZ504879A (en) | 1997-12-04 | 1998-12-04 | Instrument for engaging a power cell |
NZ524206A NZ524206A (en) | 1997-12-04 | 1998-12-04 | Instrument for determining the concentration of a medically significant component of a sample |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
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NZ524204A NZ524204A (en) | 1997-12-04 | 1998-12-04 | Instrument for the determination of physical and biological parameters such as temperature and concentration of glucose |
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US (1) | US6635167B1 (en) |
EP (2) | EP1036316B1 (en) |
JP (10) | JP3443095B2 (en) |
AU (1) | AU737787B2 (en) |
CA (4) | CA2547296C (en) |
NZ (4) | NZ504879A (en) |
WO (1) | WO1999028736A1 (en) |
Families Citing this family (145)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6826827B1 (en) | 1994-12-29 | 2004-12-07 | Tessera, Inc. | Forming conductive posts by selective removal of conductive material |
US8071384B2 (en) | 1997-12-22 | 2011-12-06 | Roche Diagnostics Operations, Inc. | Control and calibration solutions and methods for their use |
US6949816B2 (en) | 2003-04-21 | 2005-09-27 | Motorola, Inc. | Semiconductor component having first surface area for electrically coupling to a semiconductor chip and second surface area for electrically coupling to a substrate, and method of manufacturing same |
US8688188B2 (en) | 1998-04-30 | 2014-04-01 | Abbott Diabetes Care Inc. | Analyte monitoring device and methods of use |
US8974386B2 (en) | 1998-04-30 | 2015-03-10 | Abbott Diabetes Care Inc. | Analyte monitoring device and methods of use |
US8346337B2 (en) | 1998-04-30 | 2013-01-01 | Abbott Diabetes Care Inc. | Analyte monitoring device and methods of use |
US8480580B2 (en) | 1998-04-30 | 2013-07-09 | Abbott Diabetes Care Inc. | Analyte monitoring device and methods of use |
US9066695B2 (en) | 1998-04-30 | 2015-06-30 | Abbott Diabetes Care Inc. | Analyte monitoring device and methods of use |
US6175752B1 (en) | 1998-04-30 | 2001-01-16 | Therasense, Inc. | Analyte monitoring device and methods of use |
US8465425B2 (en) | 1998-04-30 | 2013-06-18 | Abbott Diabetes Care Inc. | Analyte monitoring device and methods of use |
DE19952215C2 (en) * | 1999-10-29 | 2001-10-31 | Roche Diagnostics Gmbh | Test element analysis system |
US6616819B1 (en) * | 1999-11-04 | 2003-09-09 | Therasense, Inc. | Small volume in vitro analyte sensor and methods |
US6560471B1 (en) | 2001-01-02 | 2003-05-06 | Therasense, Inc. | Analyte monitoring device and methods of use |
US7041468B2 (en) | 2001-04-02 | 2006-05-09 | Therasense, Inc. | Blood glucose tracking apparatus and methods |
AU2002300223B2 (en) * | 2001-08-13 | 2008-12-11 | Bayer Corporation | Mechanical Mechanism for a Blood Glucose Sensor Dispensing Instrument |
JP3805664B2 (en) | 2001-11-01 | 2006-08-02 | 株式会社マキタ | Battery pack |
US7022072B2 (en) * | 2001-12-27 | 2006-04-04 | Medtronic Minimed, Inc. | System for monitoring physiological characteristics |
KR100485671B1 (en) * | 2002-09-30 | 2005-04-27 | 주식회사 인포피아 | A measuring instrument for biosensor |
US20040118704A1 (en) * | 2002-12-19 | 2004-06-24 | Yi Wang | Analyte test intrument having improved versatility |
AU2003303597A1 (en) | 2002-12-31 | 2004-07-29 | Therasense, Inc. | Continuous glucose monitoring system and methods of use |
US8771183B2 (en) | 2004-02-17 | 2014-07-08 | Abbott Diabetes Care Inc. | Method and system for providing data communication in continuous glucose monitoring and management system |
US7587287B2 (en) | 2003-04-04 | 2009-09-08 | Abbott Diabetes Care Inc. | Method and system for transferring analyte test data |
US7679407B2 (en) | 2003-04-28 | 2010-03-16 | Abbott Diabetes Care Inc. | Method and apparatus for providing peak detection circuitry for data communication systems |
JP2007526440A (en) * | 2003-06-03 | 2007-09-13 | バイエル・ヘルスケア・エルエルシー | Portable medical diagnostic device |
US7645421B2 (en) | 2003-06-20 | 2010-01-12 | Roche Diagnostics Operations, Inc. | System and method for coding information on a biosensor test strip |
US8148164B2 (en) | 2003-06-20 | 2012-04-03 | Roche Diagnostics Operations, Inc. | System and method for determining the concentration of an analyte in a sample fluid |
US7645373B2 (en) | 2003-06-20 | 2010-01-12 | Roche Diagnostic Operations, Inc. | System and method for coding information on a biosensor test strip |
US7488601B2 (en) | 2003-06-20 | 2009-02-10 | Roche Diagnostic Operations, Inc. | System and method for determining an abused sensor during analyte measurement |
US8058077B2 (en) | 2003-06-20 | 2011-11-15 | Roche Diagnostics Operations, Inc. | Method for coding information on a biosensor test strip |
US7718439B2 (en) | 2003-06-20 | 2010-05-18 | Roche Diagnostics Operations, Inc. | System and method for coding information on a biosensor test strip |
US8206565B2 (en) | 2003-06-20 | 2012-06-26 | Roche Diagnostics Operation, Inc. | System and method for coding information on a biosensor test strip |
US7452457B2 (en) | 2003-06-20 | 2008-11-18 | Roche Diagnostics Operations, Inc. | System and method for analyte measurement using dose sufficiency electrodes |
CA3090413C (en) * | 2004-06-04 | 2023-10-10 | Abbott Diabetes Care Inc. | Glucose monitoring and graphical representations in a data management system |
US7453157B2 (en) | 2004-06-25 | 2008-11-18 | Tessera, Inc. | Microelectronic packages and methods therefor |
US8029441B2 (en) | 2006-02-28 | 2011-10-04 | Abbott Diabetes Care Inc. | Analyte sensor transmitter unit configuration for a data monitoring and management system |
US7545272B2 (en) | 2005-02-08 | 2009-06-09 | Therasense, Inc. | RF tag on test strips, test strip vials and boxes |
US20060233666A1 (en) * | 2005-04-15 | 2006-10-19 | Agamatrix, Inc. | Visual display for meter testing bodily fluids |
US7768408B2 (en) | 2005-05-17 | 2010-08-03 | Abbott Diabetes Care Inc. | Method and system for providing data management in data monitoring system |
WO2007027691A1 (en) | 2005-08-31 | 2007-03-08 | University Of Virginia Patent Foundation | Improving the accuracy of continuous glucose sensors |
US7583190B2 (en) | 2005-10-31 | 2009-09-01 | Abbott Diabetes Care Inc. | Method and apparatus for providing data communication in data monitoring and management systems |
US8346335B2 (en) | 2008-03-28 | 2013-01-01 | Abbott Diabetes Care Inc. | Analyte sensor calibration management |
US7801582B2 (en) | 2006-03-31 | 2010-09-21 | Abbott Diabetes Care Inc. | Analyte monitoring and management system and methods therefor |
US9339217B2 (en) | 2011-11-25 | 2016-05-17 | Abbott Diabetes Care Inc. | Analyte monitoring system and methods of use |
US9326709B2 (en) | 2010-03-10 | 2016-05-03 | Abbott Diabetes Care Inc. | Systems, devices and methods for managing glucose levels |
US8478557B2 (en) | 2009-07-31 | 2013-07-02 | Abbott Diabetes Care Inc. | Method and apparatus for providing analyte monitoring system calibration accuracy |
US9392969B2 (en) | 2008-08-31 | 2016-07-19 | Abbott Diabetes Care Inc. | Closed loop control and signal attenuation detection |
US8219173B2 (en) | 2008-09-30 | 2012-07-10 | Abbott Diabetes Care Inc. | Optimizing analyte sensor calibration |
US7620438B2 (en) | 2006-03-31 | 2009-11-17 | Abbott Diabetes Care Inc. | Method and system for powering an electronic device |
US20080071157A1 (en) | 2006-06-07 | 2008-03-20 | Abbott Diabetes Care, Inc. | Analyte monitoring system and method |
US7628085B2 (en) | 2006-11-17 | 2009-12-08 | Sru Biosystems, Inc. | Simultaneous aspirator and dispenser for multiwell plates and similar devices |
WO2008082987A2 (en) * | 2006-12-26 | 2008-07-10 | Abbott Diabetes Care Inc | Analyte meter protectors and methods |
US20080199894A1 (en) | 2007-02-15 | 2008-08-21 | Abbott Diabetes Care, Inc. | Device and method for automatic data acquisition and/or detection |
US8123686B2 (en) | 2007-03-01 | 2012-02-28 | Abbott Diabetes Care Inc. | Method and apparatus for providing rolling data in communication systems |
CN104069567A (en) | 2007-03-19 | 2014-10-01 | 茵苏莱恩医药有限公司 | Drug delivery device |
US9220837B2 (en) | 2007-03-19 | 2015-12-29 | Insuline Medical Ltd. | Method and device for drug delivery |
US8622991B2 (en) | 2007-03-19 | 2014-01-07 | Insuline Medical Ltd. | Method and device for drug delivery |
US8758245B2 (en) * | 2007-03-20 | 2014-06-24 | Lifescan, Inc. | Systems and methods for pattern recognition in diabetes management |
US20080237142A1 (en) * | 2007-04-02 | 2008-10-02 | Battelle Energy Alliance, Llc | Systems and methods for concentrating substances in fluid samples |
ES2784736T3 (en) | 2007-04-14 | 2020-09-30 | Abbott Diabetes Care Inc | Procedure and apparatus for providing data processing and control in a medical communication system |
US9204827B2 (en) | 2007-04-14 | 2015-12-08 | Abbott Diabetes Care Inc. | Method and apparatus for providing data processing and control in medical communication system |
US9008743B2 (en) | 2007-04-14 | 2015-04-14 | Abbott Diabetes Care Inc. | Method and apparatus for providing data processing and control in medical communication system |
US8140142B2 (en) | 2007-04-14 | 2012-03-20 | Abbott Diabetes Care Inc. | Method and apparatus for providing data processing and control in medical communication system |
WO2009096992A1 (en) | 2007-04-14 | 2009-08-06 | Abbott Diabetes Care, Inc. | Method and apparatus for providing data processing and control in medical communication system |
US8456301B2 (en) | 2007-05-08 | 2013-06-04 | Abbott Diabetes Care Inc. | Analyte monitoring system and methods |
US8461985B2 (en) | 2007-05-08 | 2013-06-11 | Abbott Diabetes Care Inc. | Analyte monitoring system and methods |
US7928850B2 (en) | 2007-05-08 | 2011-04-19 | Abbott Diabetes Care Inc. | Analyte monitoring system and methods |
US8665091B2 (en) | 2007-05-08 | 2014-03-04 | Abbott Diabetes Care Inc. | Method and device for determining elapsed sensor life |
US10002233B2 (en) | 2007-05-14 | 2018-06-19 | Abbott Diabetes Care Inc. | Method and apparatus for providing data processing and control in a medical communication system |
US8103471B2 (en) | 2007-05-14 | 2012-01-24 | Abbott Diabetes Care Inc. | Method and apparatus for providing data processing and control in a medical communication system |
US8560038B2 (en) | 2007-05-14 | 2013-10-15 | Abbott Diabetes Care Inc. | Method and apparatus for providing data processing and control in a medical communication system |
US9125548B2 (en) | 2007-05-14 | 2015-09-08 | Abbott Diabetes Care Inc. | Method and apparatus for providing data processing and control in a medical communication system |
US8444560B2 (en) | 2007-05-14 | 2013-05-21 | Abbott Diabetes Care Inc. | Method and apparatus for providing data processing and control in a medical communication system |
US8600681B2 (en) | 2007-05-14 | 2013-12-03 | Abbott Diabetes Care Inc. | Method and apparatus for providing data processing and control in a medical communication system |
US8239166B2 (en) | 2007-05-14 | 2012-08-07 | Abbott Diabetes Care Inc. | Method and apparatus for providing data processing and control in a medical communication system |
US8260558B2 (en) | 2007-05-14 | 2012-09-04 | Abbott Diabetes Care Inc. | Method and apparatus for providing data processing and control in a medical communication system |
ES2693097T3 (en) | 2007-05-30 | 2018-12-07 | Ascensia Diabetes Care Holdings Ag | System and method for managing health data |
JP5680960B2 (en) | 2007-06-21 | 2015-03-04 | アボット ダイアベティス ケア インコーポレイテッドAbbott Diabetes Care Inc. | Health care device and method |
EP2166928B1 (en) | 2007-06-21 | 2018-09-12 | Abbott Diabetes Care Inc. | Health monitor |
US8160900B2 (en) | 2007-06-29 | 2012-04-17 | Abbott Diabetes Care Inc. | Analyte monitoring and management device and method to analyze the frequency of user interaction with the device |
US8834366B2 (en) | 2007-07-31 | 2014-09-16 | Abbott Diabetes Care Inc. | Method and apparatus for providing analyte sensor calibration |
MX338871B (en) | 2007-12-10 | 2016-05-04 | Bayer Healthcare Llc | Interface for a health measurement and monitoring system. |
US8409133B2 (en) | 2007-12-18 | 2013-04-02 | Insuline Medical Ltd. | Drug delivery device with sensor for closed-loop operation |
US20090164239A1 (en) | 2007-12-19 | 2009-06-25 | Abbott Diabetes Care, Inc. | Dynamic Display Of Glucose Information |
US7826382B2 (en) | 2008-05-30 | 2010-11-02 | Abbott Diabetes Care Inc. | Close proximity communication device and methods |
JP5487467B2 (en) | 2008-06-16 | 2014-05-07 | パナソニックヘルスケア株式会社 | Analytical object measuring method, biosensor and measuring instrument |
JP4582210B2 (en) | 2008-06-20 | 2010-11-17 | ソニー株式会社 | Semiconductor laser, semiconductor laser manufacturing method, optical disc apparatus, and optical pickup |
WO2010040090A2 (en) * | 2008-10-03 | 2010-04-08 | Bayer Healthcare Llc | System and method for predicting ambient temperature in a fluid analyte meter |
ES2719493T3 (en) * | 2008-10-21 | 2019-07-10 | Lifescan Inc | Method and analyte evaluation system |
US8226890B2 (en) * | 2008-11-06 | 2012-07-24 | Roche Diagnostics Operations, Inc. | Diagnostic device with display module and leveraged component connections |
CN102245137A (en) | 2008-11-07 | 2011-11-16 | 茵苏莱恩医药有限公司 | Device and method for drug delivery |
US20100198034A1 (en) | 2009-02-03 | 2010-08-05 | Abbott Diabetes Care Inc. | Compact On-Body Physiological Monitoring Devices and Methods Thereof |
EP2636751A3 (en) * | 2009-03-20 | 2013-12-18 | Roche Diagniostics GmbH | Method for determining a body fluid |
US8497777B2 (en) | 2009-04-15 | 2013-07-30 | Abbott Diabetes Care Inc. | Analyte monitoring system having an alert |
WO2010127050A1 (en) | 2009-04-28 | 2010-11-04 | Abbott Diabetes Care Inc. | Error detection in critical repeating data in a wireless sensor system |
EP2424426B1 (en) | 2009-04-29 | 2020-01-08 | Abbott Diabetes Care, Inc. | Method and system for providing data communication in continuous glucose monitoring and management system |
EP2425209A4 (en) | 2009-04-29 | 2013-01-09 | Abbott Diabetes Care Inc | Method and system for providing real time analyte sensor calibration with retrospective backfill |
US9184490B2 (en) | 2009-05-29 | 2015-11-10 | Abbott Diabetes Care Inc. | Medical device antenna systems having external antenna configurations |
CA2957078C (en) | 2009-06-30 | 2019-04-30 | Lifescan, Inc | Analyte testing methods and device for calculating basal insulin therapy |
US8894933B2 (en) * | 2009-08-06 | 2014-11-25 | Roche Diagnostics Operations, Inc. | Portable handheld medical diagnostic devices |
CN105686807B (en) | 2009-08-31 | 2019-11-15 | 雅培糖尿病护理公司 | Medical Devices |
WO2011026148A1 (en) * | 2009-08-31 | 2011-03-03 | Abbott Diabetes Care Inc. | Analyte monitoring system and methods for managing power and noise |
DK3988470T3 (en) | 2009-08-31 | 2023-08-28 | Abbott Diabetes Care Inc | Display devices for a medical device |
EP2644088B1 (en) | 2009-09-29 | 2017-01-18 | Lifescan Scotland Limited | Analyte testing method and device for diabetes management |
KR101722417B1 (en) | 2010-02-25 | 2017-04-03 | 라이프스캔 스코트랜드 리미티드 | Analyte testing method and system with high and low blood glucose trends notification |
US8736273B2 (en) * | 2010-04-15 | 2014-05-27 | Lg Chem, Ltd. | Testing system and method for testing a battery cell |
US8635046B2 (en) | 2010-06-23 | 2014-01-21 | Abbott Diabetes Care Inc. | Method and system for evaluating analyte sensor response characteristics |
WO2012035725A1 (en) * | 2010-09-16 | 2012-03-22 | パナソニック株式会社 | Biological sample measuring device for medical institutions |
US8801275B2 (en) | 2010-09-23 | 2014-08-12 | Bayer Healthcare Llc | System and apparatus for determining ambient temperatures for a fluid analyte system |
WO2012048168A2 (en) | 2010-10-07 | 2012-04-12 | Abbott Diabetes Care Inc. | Analyte monitoring devices and methods |
US10136845B2 (en) | 2011-02-28 | 2018-11-27 | Abbott Diabetes Care Inc. | Devices, systems, and methods associated with analyte monitoring devices and devices incorporating the same |
EP2680754B1 (en) | 2011-02-28 | 2019-04-24 | Abbott Diabetes Care, Inc. | Devices, systems, and methods associated with analyte monitoring devices and devices incorporating the same |
WO2012157220A1 (en) | 2011-05-13 | 2012-11-22 | パナソニック株式会社 | Biological information measurement device |
US9622691B2 (en) | 2011-10-31 | 2017-04-18 | Abbott Diabetes Care Inc. | Model based variable risk false glucose threshold alarm prevention mechanism |
US9069536B2 (en) | 2011-10-31 | 2015-06-30 | Abbott Diabetes Care Inc. | Electronic devices having integrated reset systems and methods thereof |
CA2840640C (en) | 2011-11-07 | 2020-03-24 | Abbott Diabetes Care Inc. | Analyte monitoring device and methods |
US8710993B2 (en) | 2011-11-23 | 2014-04-29 | Abbott Diabetes Care Inc. | Mitigating single point failure of devices in an analyte monitoring system and methods thereof |
US9317656B2 (en) | 2011-11-23 | 2016-04-19 | Abbott Diabetes Care Inc. | Compatibility mechanisms for devices in a continuous analyte monitoring system and methods thereof |
US8728298B2 (en) * | 2012-01-18 | 2014-05-20 | SAND COUNTY BIOTECHNOLOGY, Inc. | Test method for the ketone number of an animal specimen |
US10132793B2 (en) | 2012-08-30 | 2018-11-20 | Abbott Diabetes Care Inc. | Dropout detection in continuous analyte monitoring data during data excursions |
US9968306B2 (en) | 2012-09-17 | 2018-05-15 | Abbott Diabetes Care Inc. | Methods and apparatuses for providing adverse condition notification with enhanced wireless communication range in analyte monitoring systems |
WO2014052136A1 (en) | 2012-09-26 | 2014-04-03 | Abbott Diabetes Care Inc. | Method and apparatus for improving lag correction during in vivo measurement of analyte concentration with analyte concentration variability and range data |
US9351670B2 (en) | 2012-12-31 | 2016-05-31 | Abbott Diabetes Care Inc. | Glycemic risk determination based on variability of glucose levels |
US10383580B2 (en) | 2012-12-31 | 2019-08-20 | Abbott Diabetes Care Inc. | Analysis of glucose median, variability, and hypoglycemia risk for therapy guidance |
US9474475B1 (en) | 2013-03-15 | 2016-10-25 | Abbott Diabetes Care Inc. | Multi-rate analyte sensor data collection with sample rate configurable signal processing |
US10076285B2 (en) | 2013-03-15 | 2018-09-18 | Abbott Diabetes Care Inc. | Sensor fault detection using analyte sensor data pattern comparison |
CA2895538A1 (en) | 2013-03-15 | 2014-09-18 | Abbott Diabetes Care Inc. | System and method to manage diabetes based on glucose median, glucose variability, and hypoglycemic risk |
KR101743382B1 (en) | 2013-03-15 | 2017-06-02 | 에프. 호프만-라 로슈 아게 | Methods of detecting high antioxidant levels during electrochemical measurements and failsafing an analyte concentration therefrom as well as devices, apparatuses and systems incorporting the same |
US10433773B1 (en) | 2013-03-15 | 2019-10-08 | Abbott Diabetes Care Inc. | Noise rejection methods and apparatus for sparsely sampled analyte sensor data |
KR101736651B1 (en) | 2013-03-15 | 2017-05-16 | 에프. 호프만-라 로슈 아게 | Methods of using information from recovery pulses in electrochemical analyte measurements as well as devices, apparatuses and systems incorporating the same |
CA2900883C (en) | 2013-03-15 | 2017-10-24 | F. Hoffmann-La Roche Ag | Methods of failsafing electrochemical measurements of an analyte as well as devices, apparatuses and systems incorporating the same |
KR101727447B1 (en) | 2013-03-15 | 2017-04-14 | 에프. 호프만-라 로슈 아게 | Methods of scaling data used to construct biosensor algorithms as well as devices, apparatuses and systems incorporating the same |
US20150096888A1 (en) * | 2013-10-07 | 2015-04-09 | Roche Diagnostics Operations, Inc. | bG METER LENS ATTACHMENT AND SEAL |
WO2015065390A1 (en) * | 2013-10-30 | 2015-05-07 | Draeger Safety, Inc. | Drive system for gas detection system |
US9442089B2 (en) * | 2013-12-23 | 2016-09-13 | Lifescan Scotland Limited | Analyte meter test strip detection |
US9814389B2 (en) | 2013-12-31 | 2017-11-14 | Senseonics, Incorporated | Continuous analyte monitoring system |
WO2015153482A1 (en) | 2014-03-30 | 2015-10-08 | Abbott Diabetes Care Inc. | Method and apparatus for determining meal start and peak events in analyte monitoring systems |
US9841391B2 (en) * | 2014-09-09 | 2017-12-12 | LifeSan Scotland Limited | Hand-held test meter with integrated thermal channel |
US10008854B2 (en) | 2015-02-19 | 2018-06-26 | Enphase Energy, Inc. | Method and apparatus for time-domain droop control with integrated phasor current control |
CN113349766A (en) | 2015-07-10 | 2021-09-07 | 雅培糖尿病护理公司 | System, device and method for dynamic glucose curve response to physiological parameters |
KR102373815B1 (en) * | 2015-08-31 | 2022-03-14 | 삼성전자주식회사 | Test Apparatus and Control Method thereof |
JP6927678B2 (en) * | 2016-08-18 | 2021-09-01 | ラピスセミコンダクタ株式会社 | Semiconductor devices, communication systems and initialization methods |
WO2018067235A1 (en) | 2016-10-05 | 2018-04-12 | Roche Diabetes Care, Inc. | Detection reagents and electrode arrangements for multi-analyte diagnostic test elements, as well as methods of using the same |
US10388572B2 (en) | 2017-03-06 | 2019-08-20 | International Business Machines Corporation | Integrating metal-insulator-metal capacitors with fabrication of vertical field effect transistors |
CN107063320A (en) * | 2017-03-09 | 2017-08-18 | 谢博 | A kind of bio-detector being convenient for carrying |
EP3600014A4 (en) | 2017-03-21 | 2020-10-21 | Abbott Diabetes Care Inc. | Methods, devices and system for providing diabetic condition diagnosis and therapy |
Family Cites Families (50)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3577137A (en) * | 1968-12-31 | 1971-05-04 | Texas Instruments Inc | Temperature compensated electronic display |
US3829203A (en) | 1973-05-14 | 1974-08-13 | Mosler Safe Co | Film cassette |
US4032729A (en) * | 1973-12-21 | 1977-06-28 | Rockwell International Corporation | Low profile keyboard switch having panel hinged actuators and cantilevered beam snap acting contacts |
US4007479A (en) | 1976-03-29 | 1977-02-08 | Honeywell Information Systems, Inc. | Fixture for an integrated circuit chip |
JPS58174860A (en) | 1982-04-07 | 1983-10-13 | Toshiba Corp | Charge level measuring apparatus |
JPH0737946B2 (en) * | 1983-08-05 | 1995-04-26 | 株式会社京都第一科学 | A device that measures body fluid components and stores and manages test data |
JPS61120174A (en) | 1984-11-15 | 1986-06-07 | Canon Inc | Image forming device |
DE3688142T2 (en) * | 1985-01-25 | 1993-07-22 | Mallinckrodt Sensor Syst | DEVICE FOR DETECTING OR MEASURING CHEMICAL COMPONENTS. |
JPS61179733A (en) * | 1985-02-05 | 1986-08-12 | 旭硝子株式会社 | Laminate and manufacture thereof |
JPS62202774A (en) | 1985-11-27 | 1987-09-07 | Pilot Pen Co Ltd:The | Polishing method for printing tip of dot wire or dot hammer |
JPS6343355A (en) | 1986-08-08 | 1988-02-24 | Nec Corp | Socket for ic |
JPH0750057B2 (en) * | 1987-01-30 | 1995-05-31 | 株式会社堀場製作所 | Physiological correlation value measuring device |
US5074977A (en) * | 1987-05-05 | 1991-12-24 | The Washington Technology Center | Digital biosensors and method of using same |
US5001417A (en) * | 1987-06-01 | 1991-03-19 | Abbott Laboratories | Apparatus for measuring electrolytes utilizing optical signals related to the concentration of the electrolytes |
JPS6450950A (en) * | 1987-08-22 | 1989-02-27 | Matsushita Electric Works Ltd | Apparatus for measuring component in liquid |
JPH02220375A (en) * | 1989-02-20 | 1990-09-03 | Omron Tateisi Electron Co | Biochemical measuring instrument |
US5053199A (en) | 1989-02-21 | 1991-10-01 | Boehringer Mannheim Corporation | Electronically readable information carrier |
JPH0631369Y2 (en) * | 1989-05-24 | 1994-08-22 | 横河電機株式会社 | Waterproof tact switch |
US5250262A (en) * | 1989-11-22 | 1993-10-05 | Vettest S.A. | Chemical analyzer |
US5288636A (en) | 1989-12-15 | 1994-02-22 | Boehringer Mannheim Corporation | Enzyme electrode system |
US5508171A (en) | 1989-12-15 | 1996-04-16 | Boehringer Mannheim Corporation | Assay method with enzyme electrode system |
US4963814A (en) | 1989-12-15 | 1990-10-16 | Boehringer Mannheim Corporation | Regulated bifurcated power supply |
US4999582A (en) | 1989-12-15 | 1991-03-12 | Boehringer Mannheim Corp. | Biosensor electrode excitation circuit |
US4999632A (en) | 1989-12-15 | 1991-03-12 | Boehringer Mannheim Corporation | Analog to digital conversion with noise reduction |
JPH03239958A (en) * | 1990-02-17 | 1991-10-25 | Omron Corp | Biochemical measuring instrument |
JPH0423054A (en) | 1990-05-17 | 1992-01-27 | Mitsubishi Electric Corp | Cache memory device |
JPH04254748A (en) | 1991-02-05 | 1992-09-10 | Omron Corp | Measuring device of biochemical substance |
US5246858A (en) * | 1991-02-27 | 1993-09-21 | Boehringer Mannheim Corporation | Apparatus and method for analyzing a body fluid |
GB9107193D0 (en) * | 1991-04-05 | 1991-05-22 | Wilson Robert | Analytical devices |
US5127849A (en) * | 1991-05-28 | 1992-07-07 | Motorola, Inc. | Environmentally sealed battery connector |
DE4123348A1 (en) * | 1991-07-15 | 1993-01-21 | Boehringer Mannheim Gmbh | ELECTROCHEMICAL ANALYSIS SYSTEM |
FR2701117B1 (en) * | 1993-02-04 | 1995-03-10 | Asulab Sa | Electrochemical measurement system with multizone sensor, and its application to glucose measurement. |
US5405511A (en) * | 1993-06-08 | 1995-04-11 | Boehringer Mannheim Corporation | Biosensing meter with ambient temperature estimation method and system |
US5366609A (en) | 1993-06-08 | 1994-11-22 | Boehringer Mannheim Corporation | Biosensing meter with pluggable memory key |
US5410474A (en) * | 1993-07-27 | 1995-04-25 | Miles Inc. | Buttonless memory system for an electronic measurement device |
JP3259010B2 (en) * | 1994-03-10 | 2002-02-18 | 独立行政法人産業技術総合研究所 | Enzyme electrode and measuring device using the same |
US5526280A (en) * | 1994-04-28 | 1996-06-11 | Atwood Industries, Inc. | Method and system for gas detection |
US5658801A (en) | 1994-05-03 | 1997-08-19 | Spectral Diagnostics Inc. | Medical test kit |
DE29505050U1 (en) * | 1995-03-24 | 1995-05-18 | So Henry | Switch key unit for computer keyboard boards |
JPH09161608A (en) * | 1995-12-14 | 1997-06-20 | Sony Corp | Electronic equipment |
JPH09201337A (en) * | 1996-01-25 | 1997-08-05 | Casio Comput Co Ltd | Glucose measuring device |
JP3117192B2 (en) * | 1996-04-09 | 2000-12-11 | 有限会社ホワイト | Health management meter with built-in oxidation-reduction potential measurement function |
US5718816A (en) * | 1996-05-16 | 1998-02-17 | Sendx Medical, Inc. | Locking sensor cartridge with integral fluid ports electrical connections, and pump tube |
IL124510A0 (en) * | 1996-05-17 | 1998-12-06 | Mercury Diagnostics Inc | Disposable element for use in a body fluid sampling device |
US5660791A (en) * | 1996-06-06 | 1997-08-26 | Bayer Corporation | Fluid testing sensor for use in dispensing instrument |
US5746626A (en) * | 1996-10-11 | 1998-05-05 | Bourns, Inc. | Electrical connector assembly |
US6391645B1 (en) * | 1997-05-12 | 2002-05-21 | Bayer Corporation | Method and apparatus for correcting ambient temperature effect in biosensors |
US6066243A (en) * | 1997-07-22 | 2000-05-23 | Diametrics Medical, Inc. | Portable immediate response medical analyzer having multiple testing modules |
US5931791A (en) * | 1997-11-05 | 1999-08-03 | Instromedix, Inc. | Medical patient vital signs-monitoring apparatus |
US6749997B2 (en) | 2002-05-14 | 2004-06-15 | Sandia National Laboratories | Method for providing an arbitrary three-dimensional microstructure in silicon using an anisotropic deep etch |
-
1998
- 1998-12-04 EP EP98962920A patent/EP1036316B1/en not_active Expired - Lifetime
- 1998-12-04 CA CA2547296A patent/CA2547296C/en not_active Expired - Lifetime
- 1998-12-04 EP EP10011398.4A patent/EP2270481B1/en not_active Revoked
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- 1998-12-04 WO PCT/US1998/025863 patent/WO1999028736A1/en active IP Right Grant
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2001
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2002
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